Hydrochlorothiazide
Regulatory milestones approvals, filings & regulatory actions · 3 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Approved | EU (EMA) | CoAprovel | — | 1998-10-14 | europa.eu ↗ |
| Label expansion | US (FDA) | HYDRODIURIL | — | 1992-10-28 | fda.gov ↗ |
| Approved | US (FDA) | ESIDRIX | — | 1959-02-12 | fda.gov ↗ |
Trials 236 · started per year
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 04 trials | ||||||
| Phase 0 | NCT04676399 | Feb 2022 → Dec 2026 expected | chronic pain syndrome, hypertensive disorder | University of Kansas Medical Center | Active not recruiting | No outcome recorded |
| Phase 0 | NCT03147092 | Feb 2018 → Jun 2020 | hypertensive disorder | Centro Neurológico de Pesquisa e Reabiitação, Brazil | Unknown | No outcome recorded |
| Phase 0 | NCT02744456 | Aug 2014 → Aug 2017 | hypertensive disorder | Columbia University | Completed | No outcome recorded |
| Phase 0 | NCT00649324 | Oct 2005 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 132 trials | ||||||
| Phase 1 | NCT07544888 | Nov 2025 → Mar 2026 | heart disorder, hypertensive disorder | Shaikh Zayed Hospital, Lahore | Completed | No outcome recorded |
| Phase 1 | NCT04934228 | Jul 2021 → Aug 2026 overdue | diabetes mellitus, hypertensive disorder, obesity disorder | University of Kansas Medical Center | Recruiting | No outcome recorded |
| Phase 1 | NCT04654312 | Jan → Jul 2021 | photosensitivity disease | Saarland University | Completed | No outcome recorded |
| Phase 1 | NCT06083116 | Aug → Oct 2019 | type 2 diabetes mellitus | Jiangsu HengRui Medicine Co., Ltd. | Completed | No outcome recorded |
| Phase 1 | NCT04197622 | Mar 2019 | — | Parc de Salut Mar | Completed | No outcome recorded |
| Phase 1 | NCT03629067 | Sep → Nov 2018 | — | Boryung Pharmaceutical Co., Ltd | Completed | No outcome recorded |
| Phase 1 | NCT03387657 | Jan → Mar 2018 | type 2 diabetes mellitus | Sanofi | Completed | No outcome recorded |
| Phase 1 | NCT03390465 | Dec 2017 → Jan 2018 | — | Boryung Pharmaceutical Co., Ltd | Completed | No outcome recorded |
| Phase 1 | NCT02183675 | Jul → Oct 2014 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1 | NCT02094924 | Apr → May 2014 | hypertensive disorder | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT03889145 | Dec 2013 → Feb 2014 | — | IlDong Pharmaceutical Co Ltd | Completed | No outcome recorded |
| Phase 1 | NCT01692717 | Feb → May 2013 | — | Azidus Brasil | Completed | No outcome recorded |
| Phase 1 | NCT02962258 | May → Jun 2011 | — | Torrent Pharmaceuticals Limited | Completed | No outcome recorded |
| Phase 1 | NCT01294631 | Mar → Jul 2011 | — | Johnson & Johnson Pharmaceutical Research & Development, L.L.C. | Completed | No outcome recorded |
| Phase 1 | NCT01198249 | Sep 2010 → Feb 2011 | essential hypertension | Yonsei University | Completed | No outcome recorded |
| Phase 1 | NCT00871871 | Mar 2009 → Feb 2010 | hypertensive disorder | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 1 | NCT02276378 | Jul → Aug 2008 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1 | NCT00671424 | Mar → May 2008 | type 2 diabetes mellitus | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT01020214 | Nov 2006 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT01019590 | Nov 2006 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT01149486 | Jan → Feb 2004 | — | Teva Pharmaceuticals USA | Completed | No outcome recorded |
| Phase 1 | NCT02262780 | Dec 2003 → Feb 2004 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1 | NCT00834067 | Oct → Nov 2003 | — | Teva Pharmaceuticals USA | Completed | No outcome recorded |
| Phase 1 | NCT00835042 | Oct → Nov 2003 | — | Teva Pharmaceuticals USA | Completed | No outcome recorded |
| Phase 1 | NCT00648011 | Aug 2003 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00649441 | Aug → Sep 2003 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT02262572 | Apr → Aug 2003 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1 | NCT00649233 | Jan → Feb 2003 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00649038 | Dec 2002 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00649597 | Nov → Dec 2002 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00223717 | Jan 2001 → Jan 2017 | hypertensive disorder | Vanderbilt University | Completed | No outcome recorded |
| Phase 1 | NCT02176512 | Sep → Oct 1998 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 213 trials | ||||||
| Phase 2 | NCT07634068 | Jun 2026 → Jun 2027 expected | cerebrovascular disorder | Huashan Hospital | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT05897372 | Aug 2023 → Sep 2024 | diabetic kidney disease | Iain Bressendorff | Terminated | No outcome recorded |
| Phase 2 | NCT03329599 | Feb 2019 → Dec 2021 | atherosclerosis | Northern California Institute of Research and Education | Completed | No outcome recorded |
| Phase 2 | NCT03024476 | Sep 2016 → Dec 2017 | hypertensive disorder, ischemic stroke | Seoul National University Bundang Hospital | Completed | No outcome recorded |
| Phase 2 | NCT02278471 | Dec 2015 → Jun 2018 | hyperlipidemia, hypertensive disorder | Vanderbilt University | Completed | No outcome recorded |
| Phase 2 | NCT02222480 | Oct 2014 → May 2015 | essential hypertension | Boryung Pharmaceutical Co., Ltd | Completed | No outcome recorded |
| Phase 2 | NCT01480791 | Jan 2012 → Dec 2013 | diabetes mellitus, hypertensive disorder | Sir Mortimer B. Davis - Jewish General Hospital | Withdrawn | No outcome recorded |
| Phase 2 | NCT01302899 | Jan → Dec 2011 | — | Novartis Pharmaceuticals | Terminated | No outcome recorded |
| Phase 2 | NCT00567307 | Jan → Dec 2009 | cardiovascular disorder | Wake Forest University Health Sciences | Completed | No outcome recorded |
| Phase 2 | NCT00388388 | Mar 2007 → Dec 2009 | hypertensive disorder, prediabetes syndrome | Sir Mortimer B. Davis - Jewish General Hospital | Terminated | No outcome recorded |
| Phase 2 | NCT00603590 | Nov 2006 → Jun 2008 | heart disorder, hyperlipidemia, hypertensive disorder | Tehran University of Medical Sciences | Completed | No outcome recorded |
| Phase 2 | NCT00374855 | Sep → Nov 2006 | hypertensive disorder | Eli Lilly and Company | Completed | No outcome recorded |
| Phase 2 | NCT00153049 | Jun 2004 → Jun 2005 | essential hypertension | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2/32 trials | ||||||
| Phase 2/3 | NCT07469722 | Mar 2026 → Jan 2028 expected | congestive heart failure | Hospital de Clinicas de Porto Alegre | Not yet recruiting | No outcome recorded |
| Phase 2/3 | NCT00638482 | Jul 2003 → Dec 2005 | Dent disease, nephrolithiasis | Assistance Publique - Hôpitaux de Paris | Terminated | No outcome recorded |
| Phase 379 trials | ||||||
| Phase 3 | NCT05963568 | Apr 2026 → Jan 2029 expected | stroke disorder | Northern California Institute of Research and Education | Recruiting | No outcome recorded |
| Phase 3 | NCT07008365 | Mar 2025 → Nov 2026 expected | cardio-renal syndrome, congestive heart failure | Aragon Health Research Institute (IISAragon) | Recruiting | No outcome recorded |
| Phase 3 | NCT04465123 | Aug 2020 → Jul 2022 | acute kidney injury, heart failure | Chiang Mai University | Unknown | No outcome recorded |
| Phase 3 | NCT03057431 | Mar 2017 → Dec 2021 | nephrolithiasis | Insel Gruppe AG, University Hospital Bern | Completed | No outcome recorded |
| Phase 3 | NCT03246555 | Jul 2016 → Aug 2019 | — | Boryung Pharmaceutical Co., Ltd | Completed | No outcome recorded |
| Phase 3 | NCT03249285 | Mar 2016 → Mar 2018 | essential hypertension | Ospedale San Raffaele | Unknown | No outcome recorded |
| Phase 3 | NCT03459560 | Dec 2015 → Mar 2022 | cardiovascular disorder | Tehran University of Medical Sciences | Unknown | No outcome recorded |
| Phase 3 | NCT02738632 | May 2015 → Aug 2016 | essential hypertension | IlDong Pharmaceutical Co Ltd | Completed | No outcome recorded |
| Phase 3 | NCT02277691 | Nov 2014 → Apr 2016 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 3 | NCT01975246 | Nov 2013 → Jun 2014 | essential hypertension | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT01911780 | Jul 2013 → Jan 2015 | essential hypertension | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02466490 | Apr 2013 → Feb 2014 | essential hypertension | Stendhal Americas, S.A. | Completed | No outcome recorded |
| Phase 3 | NCT01313702 | Oct 2012 → Apr 2014 | cardiovascular disorder | Hospital do Coracao | Withdrawn | No outcome recorded |
| Phase 3 | NCT01646437 | Jun 2012 → Jun 2020 | cardiovascular disorder | Population Health Research Institute | Completed | No outcome recorded |
| Phase 3 | NCT01245608 | Oct 2011 → Jan 2018 | cardiovascular disorder | Tehran University of Medical Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01307046 | Mar 2011 → Feb 2012 | essential hypertension | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT01326676 | Feb 2011 → Jul 2012 | cardiovascular disorder | Imperial College London | Withdrawn | No outcome recorded |
| Phase 3 | NCT01302691 | Jan 2011 → Apr 2012 | hypertensive disorder | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT01259297 | Jan 2011 → Nov 2012 | — | Novartis Pharmaceuticals | Terminated | No outcome recorded |
| Phase 3 | NCT01258673 | Nov 2010 → Dec 2011 | essential hypertension | Boryung Pharmaceutical Co., Ltd | Completed | No outcome recorded |
| Phase 3 | NCT01057537 | Jun 2010 → Jul 2012 | cardiovascular disorder | Imperial College London | Completed | No outcome recorded |
| Phase 3 | NCT01113047 | May → Oct 2010 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00923091 | Jun 2009 → Jan 2011 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT00902538 | Apr 2009 → Sep 2010 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT00818883 | Feb → Nov 2009 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 3 | NCT00765674 | Sep 2008 → Aug 2009 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00667719 | Jun 2008 → Oct 2009 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00705575 | Jun 2008 → Apr 2009 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00548067 | Sep 2007 → Mar 2008 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00441350 | Jul 2007 → May 2008 | hypertensive disorder | Menarini Group | Completed | No outcome recorded |
| Phase 3 | NCT00523744 | Jul → Dec 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00447603 | May → Oct 2007 | hypertensive disorder | Organon and Co | Terminated | No outcome recorded |
| Phase 3 | NCT00459056 | Apr 2007 → May 2010 | abdominal obesity-metabolic syndrome, hypertensive disorder | St. Paul Heart Clinic | Completed | No outcome recorded |
| Phase 3 | NCT00430508 | Feb 2007 → Mar 2008 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT00430950 | Feb 2007 → May 2008 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT00434967 | Jan 2007 → Jan 2008 | hypertensive disorder | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00402103 | Nov 2006 → Apr 2008 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00386607 | Oct 2006 → Jul 2008 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00387517 | Oct 2006 → Aug 2007 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00386139 | Sep 2006 → Jul 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00383929 | Sep 2006 → Aug 2007 | hypertensive disorder | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00872586 | Aug 2006 → Jul 2007 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT00355589 | Jul 2006 → Mar 2007 | essential hypertension | Pfizer | Completed | No outcome recorded |
| Phase 3 | NCT00367094 | Jul 2006 → ? | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00354991 | Jun 2006 → Apr 2007 | essential hypertension | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT00326768 | May 2006 → Aug 2007 | essential hypertension | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00338936 | May 2006 → Sep 2007 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00327587 | May 2006 → Aug 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00449111 | Mar → Sep 2006 | hypertensive disorder | Organon and Co | Terminated | No outcome recorded |
| Phase 3 | NCT00311740 | Mar → Sep 2006 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00289887 | Feb 2006 → Feb 2007 | hypertensive disorder | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00267943 | Jan 2006 → Jan 2007 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00396656 | Dec 2005 → Dec 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00273299 | Nov 2005 → Jul 2006 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00257491 | Nov 2005 → Aug 2006 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00250562 | Oct 2005 → Jun 2006 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00239369 | Oct 2005 → Aug 2006 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00546052 | Sep 2005 → Jan 2008 | hypertensive disorder, metabolic disease | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00400218 | Sep 2005 → Jul 2006 | essential hypertension | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00139698 | Sep 2005 → Jul 2006 | essential hypertension | Pfizer | Completed | No outcome recorded |
| Phase 3 | NCT00263003 | Jun 2005 → ? | hypertensive disorder | Sanofi | Completed | No outcome recorded |
| Phase 3 | NCT00146341 | Apr 2005 → Sep 2006 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00398541 | Mar 2005 → Apr 2007 | hypertensive disorder | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00144222 | Jan → Aug 2005 | essential hypertension | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00307060 | Dec 2004 → Jun 2005 | hypertensive disorder | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00171015 | Dec 2004 → Apr 2005 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00095550 | Oct 2004 → Jun 2005 | hypertensive disorder | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 3 | NCT00170989 | Sep 2004 → Jul 2005 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00095394 | Sep 2004 → May 2005 | hypertensive disorder | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 3 | NCT00241007 | Dec 2003 → Mar 2005 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00642096 | Jun 2003 → Jul 2004 | essential hypertension | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00092209 | Apr → Nov 2002 | essential hypertension | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00185172 | Jan 2002 → Jun 2005 | essential hypertension | Sankyo Pharma Gmbh | Completed | No outcome recorded |
| Phase 3 | NCT02177500 | Jan → May 2000 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02177487 | Jun 1999 → Jan 2000 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02177435 | Feb → Sep 1999 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02177422 | Jun 1998 → Nov 1999 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00000525 | Jul 1986 → Sep 1989 | cardiac arrest, hypertensive disorder, sudden arrhythmia death syndrome | University of California, San Francisco | Completed | No outcome recorded |
| Phase 3 | NCT02493322 | ? → Jun 2025 | essential hypertension | EMS | Withdrawn | No outcome recorded |
| Phase 484 trials | ||||||
| Phase 4 | NCT07593612 | Jun 2026 → Jan 2027 expected | heart failure | Lucrecia Maria Burgos | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT05917275 | Apr 2024 → Oct 2025 | essential hypertension | Radboud University Medical Center | Unknown | No outcome recorded |
| Phase 4 | NCT05443932 | Mar → Dec 2024 | urolithiasis | Medical University of Vienna | Unknown | No outcome recorded |
| Phase 4 | NCT05171686 | Feb 2023 → Oct 2025 | chronic kidney disease, hypertensive disorder | VA Office of Research and Development | Completed | No outcome recorded |
| Phase 4 | NCT05049616 | Oct 2021 → Jun 2022 | preeclampsia | The University of Texas Health Science Center, Houston | Completed | No outcome recorded |
| Phase 4 | NCT03423355 | Sep 2021 → Mar 2023 | type 2 diabetes mellitus | University Hospital Tuebingen | Withdrawn | No outcome recorded |
| Phase 4 | NCT04192110 | Aug 2020 | chronic kidney disease | VA Office of Research and Development | Withdrawn | No outcome recorded |
| Phase 4 | NCT04330300 | Apr 2020 → Jul 2021 | COVID-19, essential hypertension | National University of Ireland, Galway, Ireland | Suspended | No outcome recorded |
| Phase 4 | NCT04242758 | Jun → Dec 2019 | glucose metabolism disease, impaired renal function disease | University of Pisa | Unknown | No outcome recorded |
| Phase 4 | NCT03978884 | Jun 2019 → May 2020 | diabetes mellitus, hypertensive disorder | The University of The West Indies | Withdrawn | No outcome recorded |
| Phase 4 | NCT03892148 | May 2019 → Jan 2023 | heart failure | University Hospital, Clermont-Ferrand | Completed | No outcome recorded |
| Phase 4 | NCT03682692 | Jun 2018 → Jun 2021 | hypertensive disorder | Shanghai Jiao Tong University School of Medicine | Completed | No outcome recorded |
| Phase 4 | NCT03461003 | Apr 2018 → Nov 2020 | early onset hypertension | The University of Texas Health Science Center, Houston | Completed | No outcome recorded |
| Phase 4 | NCT03254849 | Dec 2017 → Apr 2020 | type 2 diabetes mellitus | Profil Institute for Metabolic Research GmbH | Completed | No outcome recorded |
| Phase 4 | NCT02742467 | Jun 2017 → Jun 2018 | hypertensive disorder | University of Abuja | Completed | No outcome recorded |
| Phase 4 | NCT02646397 | Feb 2016 → Dec 2017 | chronic kidney disease | Shanghai Changzheng Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT02377661 | Mar 2015 → May 2017 | hypertensive disorder | Wilhelminenspital Vienna | Completed | No outcome recorded |
| Phase 4 | NCT02710071 | Jan 2015 → Apr 2016 | essential hypertension | University of California, San Diego | Completed | No outcome recorded |
| Phase 4 | NCT02699125 | Jan 2015 → Jun 2016 | obstructive sleep apnea syndrome | University of California, San Diego | Completed | No outcome recorded |
| Phase 4 | NCT02294539 | Aug 2014 → May 2016 | hypertensive disorder | Chong-Jin Kim | Completed | No outcome recorded |
| Phase 4 | NCT02217852 | Aug 2014 → Jan 2016 | hypertensive disorder | West China Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT02100462 | Mar 2014 → Dec 2016 | hypertensive disorder | Creighton University | Unknown | No outcome recorded |
| Phase 4 | NCT01977430 | Nov 2013 → Mar 2015 | chronic kidney disease | Corporacion Parc Tauli | Unknown | No outcome recorded |
| Phase 4 | NCT01198496 | Oct 2010 → Dec 2017 | essential hypertension, stroke disorder | Biomedis International Ltd. | Unknown | No outcome recorded |
| Phase 4 | NCT01138423 | Aug 2010 → Feb 2012 | hypertensive disorder, metabolic syndrome X | UMC Utrecht | Completed | No outcome recorded |
| Phase 4 | NCT01056731 | Feb 2010 → Oct 2011 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00994617 | Jan 2010 → Dec 2014 | essential hypertension, resistant hypertension | University of Cambridge | Unknown | No outcome recorded |
| Phase 4 | NCT01070030 | Jan → Oct 2010 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT02351973 | Nov 2009 → Jul 2015 | essential hypertension | University of Cambridge | Unknown | No outcome recorded |
| Phase 4 | NCT00896389 | Oct 2009 → Dec 2012 | hypertensive disorder | University of Maryland, Baltimore | Completed | No outcome recorded |
| Phase 4 | NCT01012479 | Oct 2009 → May 2010 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 4 | NCT00902304 | Jul 2009 → Jul 2011 | hypertensive disorder | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT00931710 | Jul 2009 → Jan 2010 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00942994 | Jun 2009 → Mar 2010 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00926289 | Jun 2009 → Apr 2010 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT01819220 | Apr 2009 → Nov 2014 | hypertensive disorder | Yonsei University | Completed | No outcome recorded |
| Phase 4 | NCT00795847 | Nov 2008 → Nov 2010 | hypertensive disorder | Kurume University | Completed | No outcome recorded |
| Phase 4 | NCT00797316 | Nov 2008 → Dec 2009 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00791258 | Nov 2008 → Aug 2009 | hypertensive disorder | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00787605 | Nov 2008 → Jan 2010 | diabetes mellitus, hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00765947 | Sep 2008 → Aug 2009 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00772577 | Aug 2008 → Mar 2009 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00739596 | Jul 2008 → Mar 2009 | hypertensive disorder | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT00654745 | May 2008 → Apr 2009 | essential hypertension, type 2 diabetes mellitus | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00698646 | Apr 2008 → Jun 2009 | essential hypertension | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT00670566 | Apr 2008 → Mar 2009 | hypertensive disorder | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00687206 | Mar → May 2008 | erectile dysfunction, hypertensive disorder | Federico II University | Completed | No outcome recorded |
| Phase 4 | NCT00496834 | Feb 2008 → Sep 2009 | hypertensive disorder | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00621153 | Feb 2008 → Mar 2009 | hypertensive disorder | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT00492128 | Sep 2007 → May 2009 | hypertensive disorder | Yokohama City University Medical Center | Completed | No outcome recorded |
| Phase 4 | NCT01431508 | Aug 2007 → Jun 2009 | essential hypertension | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00457483 | Aug 2007 → Dec 2010 | essential hypertension | Radboud University Medical Center | Completed | No outcome recorded |
| Phase 4 | NCT00439738 | Dec 2006 → Nov 2007 | hypertensive disorder | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT00425997 | Dec 2006 → Oct 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00412932 | Dec 2006 → Apr 2008 | hypertensive disorder | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00430638 | Dec 2006 → Oct 2007 | hypertensive disorder | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT01425411 | Nov 2006 → Nov 2008 | hypertensive disorder, hypertensive heart disease | Mustafa Kemal University | Completed | No outcome recorded |
| Phase 4 | NCT00403481 | Nov 2006 → Nov 2007 | hypertensive disorder | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00426478 | Nov 2006 → Sep 2007 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00443612 | Sep 2006 → Oct 2008 | hypertensive disorder | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00400777 | Aug 2006 → Nov 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00890591 | Aug 2006 → Jun 2007 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00607035 | May 2006 → Apr 2008 | hypertensive disorder | Jichi Medical University | Completed | No outcome recorded |
| Phase 4 | NCT00311155 | Mar 2006 → Apr 2008 | essential hypertension | Sankyo Pharma Gmbh | Completed | No outcome recorded |
| Phase 4 | NCT00335673 | Feb → Nov 2006 | hypertensive disorder | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00280540 | Dec 2005 → Aug 2006 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00535925 | Oct 2005 → Dec 2011 | diabetic kidney disease | University of Campania Luigi Vanvitelli | Completed | No outcome recorded |
| Phase 4 | NCT00246519 | Oct 2005 → Dec 2010 | hypertensive disorder | University of Florida | Completed | No outcome recorded |
| Phase 4 | NCT00168779 | Sep 2005 → Jul 2006 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00185120 | Sep 2005 → Sep 2006 | hypertensive disorder | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00821574 | Jul 2005 → Mar 2007 | hyperlipidemia, combined, 2 | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00157963 | Feb 2005 → Feb 2006 | essential hypertension | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00170937 | Nov 2004 → Mar 2006 | hypertensive disorder, metabolic syndrome X | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00185068 | Mar → Oct 2004 | hypertensive disorder | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00171782 | Feb → Dec 2004 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00154271 | Jan 2004 → Jun 2005 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00847834 | Dec 2003 → Jun 2004 | essential hypertension | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00240448 | Sep 2003 → Jun 2004 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00171054 | Sep 2003 → Oct 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00171561 | Mar 2003 → Sep 2006 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00306696 | Oct 2002 → Jan 2004 | diabetes mellitus | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT03921736 | Jan 2000 → Mar 2001 | essential hypertension | Anna Posadzy-Małaczyńska | Completed | No outcome recorded |
| Phase 4 | NCT02172586 | Jan 2000 → Jan 2002 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00133692 | Sep 1997 → Feb 2003 | coronary artery disorder, hypertensive disorder | University of Florida | Completed | No outcome recorded |
| Phase not applicable22 trials | ||||||
| — | NCT06790927 | Feb 2025 → Dec 2026 expected | hypertensive disorder | Shanghai Jiao Tong University School of Medicine | Not yet recruiting | No outcome recorded |
| — | NCT07020104 | Jan 2025 → Dec 2039 expected | chronic kidney disease | Academic Medical Center - University of Amsterdam | Recruiting | No outcome recorded |
| — | NCT06491940 | Aug 2024 → Jul 2025 overdue | proteinuria | RESnTEC, Institute of Research | Not yet recruiting | No outcome recorded |
| — | NCT06710600 | Sep 2022 → Apr 2024 | photosensitivity disease | Medical University of Vienna | Completed | No outcome recorded |
| — | NCT04182854 | Oct 2019 → Feb 2020 | antidepressant type abuse | Capital Medical University | Unknown | No outcome recorded |
| — | NCT02765009 | Jun 2016 → Jul 2019 | — | Central Hospital, Nancy, France | Completed | No outcome recorded |
| — | NCT02255253 | Oct 2014 → Feb 2015 | hypertensive disorder | The George Institute for Global Health, China | Completed | No outcome recorded |
| — | NCT02711670 | Feb 2014 → Jun 2017 | urolithiasis | VA New York Harbor Healthcare System | Completed | No outcome recorded |
| — | NCT04371874 | Jan 2014 → Jul 2017 | hypertensive disorder | First Affiliated Hospital Xi'an Jiaotong University | Completed | No outcome recorded |
| — | NCT01858610 | Mar → Apr 2013 | — | Damanhour University | Completed | No outcome recorded |
| — | NCT01858623 | Feb → Mar 2013 | — | Damanhour University | Completed | No outcome recorded |
| — | NCT01767298 | Oct → Dec 2012 | — | Damanhour University | Completed | No outcome recorded |
| — | NCT01658657 | Oct 2012 → Jul 2014 | hypertensive disorder, proteolytic capacity of plasma | University of North Carolina, Chapel Hill | Completed | No outcome recorded |
| — | NCT01767259 | Oct → Dec 2012 | — | Damanhour University | Completed | No outcome recorded |
| — | NCT01506505 | Jul 2012 → Jul 2013 | cerebrovascular disorder, peripheral arterial disease | UMC Utrecht | Completed | No outcome recorded |
| — | NCT00822107 | Jan 2009 → Jan 2013 | Gitelman syndrome | Oregon Health and Science University | Completed | No outcome recorded |
| — | NCT00700583 | May → Jun 2008 | — | Seoul National University Hospital | Completed | No outcome recorded |
| — | NCT00424801 | Jan 2007 → Dec 2008 | coronary microvascular disorder, essential hypertension | University of Aarhus | Terminated | No outcome recorded |
| — | NCT00834600 | Dec 2005 → Oct 2011 | hypertensive disorder | The Louis & Rachel Rudin Foundation | Completed | No outcome recorded |
| — | NCT00690521 | Oct 2004 → Nov 2009 | congestive heart failure | University of New Mexico | Completed | No outcome recorded |
| — | NCT00162474 | Sep 2003 → Dec 2030 expected | — | Hadassah Medical Organization | Recruiting | No outcome recorded |
| — | NCT00247910 | Oct 2001 → Jun 2006 | hypertensive disorder | University of British Columbia | Completed | No outcome recorded |
Also used as a comparator or background therapy in 169 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 03 trials | ||||||
| Phase 0 | NCT04423627 Comparator | Jun 2021 → Jul 2025 | hypertensive disorder | University of Iowa | Completed | No outcome recorded |
| Phase 0 | NCT01804777 Comparator | Mar 2013 → Dec 2014 | hypertensive disorder, proteinuria, type 2 diabetes mellitus | University of New Mexico | Terminated | No outcome recorded |
| Phase 0 | NCT00574834 Comparator | Mar 2007 → Aug 2014 | metabolic syndrome X | University of Maryland, Baltimore | Terminated | No outcome recorded |
| Phase 111 trials | ||||||
| Phase 1 | NCT06205407 Comparator | Dec 2023 → Mar 2024 | — | Pfizer | Completed | No outcome recorded |
| Phase 1 | NCT03971929 Comparator | Jul 2019 → Sep 2020 | hypertensive disorder | Jiangsu HengRui Medicine Co., Ltd. | Completed | No outcome recorded |
| Phase 1 | NCT03032315 Comparator | Oct → Dec 2016 | — | IlDong Pharmaceutical Co Ltd | Completed | No outcome recorded |
| Phase 1 | NCT02739672 Comparator | Jan → Apr 2016 | — | IlDong Pharmaceutical Co Ltd | Completed | No outcome recorded |
| Phase 1 | NCT01370655 Comparator | Jun → Dec 2011 | hypertensive disorder | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 1 | NCT01276288 Comparator | Jan → Jun 2011 | type 2 diabetes mellitus | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1 | NCT01103245 Comparator | Mar 2010 → Jul 2012 | diabetes mellitus | Vanderbilt University Medical Center | Completed | No outcome recorded |
| Phase 1 | NCT00923533 Comparator | Mar → May 2009 | essential hypertension | Boryung Pharmaceutical Co., Ltd | Completed | No outcome recorded |
| Phase 1 | NCT01149473 Comparator | Mar → Apr 2004 | — | Teva Pharmaceuticals USA | Completed | No outcome recorded |
| Phase 1 | NCT00649688 Comparator | Jan → Feb 2003 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT02187523 Comparator | Oct → Dec 1999 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1/21 trial | ||||||
| Phase 1/2 | NCT03179163 Comparator | Jul 2016 → Aug 2022 | essential hypertension | Penn State University | Terminated | No outcome recorded |
| Phase 213 trials | ||||||
| Phase 2 | NCT06111885 Comparator | Oct 2024 → Jun 2027 expected | urolithiasis | Insel Gruppe AG, University Hospital Bern | Recruiting | No outcome recorded |
| Phase 2 | NCT03658850 Comparator | Oct 2018 → Dec 2019 | — | University of Sao Paulo | Unknown | No outcome recorded |
| Phase 2 | NCT03295734 Comparator | May 2018 → Sep 2024 | hypertensive disorder | University of Alabama at Birmingham | Completed | No outcome recorded |
| Phase 2 | NCT03198793 Background | Oct 2017 → Oct 2018 | essential hypertension | Quantum Genomics SA | Completed | No outcome recorded |
| Phase 2 | NCT02824718 Comparator | Jun 2017 → May 2020 | autosomal dominant hypocalcemia | Assistance Publique - Hôpitaux de Paris | Completed | No outcome recorded |
| Phase 2 | NCT01879527 Comparator | Mar 2014 → Apr 2016 | optic neuritis | Medical University of Vienna | Unknown | No outcome recorded |
| Phase 2 | NCT01983462 Comparator | Oct 2013 → Jun 2020 | hypertensive disorder, obesity disorder | Gary L. Pierce | Terminated | No outcome recorded |
| Phase 2 | NCT01692301 Background | Dec 2012 → Apr 2015 | hypertensive disorder | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT01256411 Background | Nov 2010 → Apr 2012 | essential hypertension | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT00976495 Comparator | Oct 2009 → Nov 2010 | type 2 diabetes mellitus | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT00806585 Comparator | Dec 2008 → Mar 2010 | hypertensive disorder, type 2 diabetes mellitus | Merck Sharp & Dohme LLC | Terminated | No outcome recorded |
| Phase 2 | NCT00605072 Comparator | Jan 2008 → Dec 2011 | cognitive impairment with or without cerebellar ataxia, hypertensive disorder | University of Southern California | Completed | No outcome recorded |
| Phase 2 | NCT00282178 Comparator | Apr 2005 → Mar 2006 | hypertensive disorder, obesity disorder | Umeå University | Completed | No outcome recorded |
| Phase 2/31 trial | ||||||
| Phase 2/3 | NCT02072330 Comparator | Mar → Dec 2013 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 346 trials | ||||||
| Phase 3 | NCT06608472 Comparator | Nov 2026 → Apr 2028 expected | essential hypertension | Eurofarma Laboratorios S.A. | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT05373264 Comparator | Jul 2024 → Jul 2030 expected | autosomal dominant polycystic kidney disease | University Medical Center Groningen | Recruiting | No outcome recorded |
| Phase 3 | NCT05920005 Comparator | Aug 2023 → Mar 2025 | hypertensive disorder | Hospital Israelita Albert Einstein | Completed | No outcome recorded |
| Phase 3 | NCT04927299 Comparator | Jun 2022 → Aug 2023 | essential hypertension | Laboratorios Silanes S.A. de C.V. | Completed | No outcome recorded |
| Phase 3 | NCT01620788 Comparator | Nov 2019 → Jul 2023 | hypertensive disorder | EMS | Suspended | No outcome recorded |
| Phase 3 | NCT03928145 Comparator | Nov 2019 → Jul 2021 | essential hypertension | Hospital de Clinicas de Porto Alegre | Unknown | No outcome recorded |
| Phase 3 | NCT03660397 Background | Aug 2018 → Jul 2019 | hypertensive disorder | Third Military Medical University | Unknown | No outcome recorded |
| Phase 3 | NCT03298802 Comparator | Nov 2017 → Apr 2025 | preeclampsia | The University of Texas Medical Branch, Galveston | Terminated | No outcome recorded |
| Phase 3 | NCT02521246 Comparator | Nov 2016 → May 2017 | essential hypertension | EMS | Withdrawn | No outcome recorded |
| Phase 3 | NCT02521233 Comparator | Nov 2016 → May 2017 | essential hypertension | EMS | Withdrawn | No outcome recorded |
| Phase 3 | NCT02900729 Background | Oct 2016 → Aug 2017 | hypertensive disorder | Shanghai WiseGain Medical Devices Co., Ltd. | Unknown | No outcome recorded |
| Phase 3 | NCT02185417 Comparator | Jun 2016 → Oct 2022 | hypertensive disorder | VA Office of Research and Development | Completed | No outcome recorded |
| Phase 3 | NCT01647932 Comparator | Oct 2014 → Dec 2019 | heart failure | Spanish Society of Internal Medicine | Completed | No outcome recorded |
| Phase 3 | NCT04952051 Comparator | Jul 2014 → Jul 2019 | hypertensive disorder | Second Affiliated Hospital, School of Medicine, Zhejiang University | Completed | No outcome recorded |
| Phase 3 | NCT01838850 Background | Apr 2013 → Aug 2014 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT01365481 Background | Aug 2011 → Sep 2015 | chronic kidney disease, hypertensive disorder | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01415505 Background | Aug 2011 → Jan 2013 | essential hypertension | Forest Laboratories | Completed | No outcome recorded |
| Phase 3 | NCT01307033 Background | Mar 2011 → Dec 2012 | hypertensive disorder | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT01309828 Comparator | Mar 2011 → Oct 2012 | — | Takeda | Completed | No outcome recorded |
| Phase 3 | NCT01271985 Comparator | Feb 2011 → Jan 2019 | cardiovascular disorder | Tehran University of Medical Sciences | Completed | No outcome recorded |
| Phase 3 | NCT01299376 Background | Jan → Nov 2011 | hypertensive disorder | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT01033071 Comparator | Jan → Oct 2010 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 3 | NCT00996281 Comparator | Oct 2009 → Nov 2011 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 3 | NCT01127217 Background | May 2009 → Mar 2010 | hypertensive disorder | Hanmi Pharmaceutical Company Limited | Completed | No outcome recorded |
| Phase 3 | NCT00867490 Background | Mar → Aug 2009 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00846365 Comparator | Mar 2009 → Jun 2010 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 3 | NCT00797862 Background | Nov 2008 → Nov 2010 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00670787 Comparator | Jun 2008 → Nov 2010 | hypertensive disorder | Kyushu University | Completed | No outcome recorded |
| Phase 3 | NCT00649389 Comparator | May 2008 → Apr 2009 | hypertensive disorder | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT00739674 Background | Feb 2008 → Jul 2009 | essential hypertension | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00695955 Background | Jun 2007 → May 2010 | essential hypertension | Takeda | Completed | No outcome recorded |
| Phase 3 | NCT00546754 Comparator | May 2007 → Apr 2009 | hypertensive disorder | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00446563 Comparator | Mar 2007 → Mar 2010 | hypertensive heart disease | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00368277 Background | Sep 2006 → Feb 2008 | essential hypertension | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT00360178 Background | Jul → Dec 2006 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00327145 Background | Mar 2006 → Jan 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00220233 Background | Apr 2005 → Aug 2007 | essential hypertension | Sankyo Pharma Gmbh | Completed | No outcome recorded |
| Phase 3 | NCT00133185 Background | Mar 2004 → Mar 2005 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00170950 Comparator | Oct 2003 → Jan 2008 | hypertensive disorder | Novartis | Terminated | No outcome recorded |
| Phase 3 | NCT00751829 Background | Jul 2003 → Oct 2004 | — | Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company | Completed | No outcome recorded |
| Phase 3 | NCT00751751 Background | Jun 2003 → Apr 2005 | essential hypertension | Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company | Completed | No outcome recorded |
| Phase 3 | NCT00185185 Background | Nov 2001 → Feb 2006 | atherosclerotic cardiovascular disease, essential hypertension | Sankyo Pharma Gmbh | Completed | No outcome recorded |
| Phase 3 | NCT02175355 Comparator | Oct 1999 → Aug 2000 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02183701 Comparator | Apr → Dec 1998 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00886600 Background | May 1991 → May 1992 | hypertensive disorder | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT02483936 Comparator | ? → Jun 2025 | essential hypertension | EMS | Withdrawn | No outcome recorded |
| Phase 471 trials | ||||||
| Phase 4 | NCT07687160 Comparator | Sep 2026 → Feb 2028 expected | hypertensive disorder | Ottawa Hospital Research Institute | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT06041529 Comparator | Oct 2023 → Feb 2026 overdue | essential hypertension | Yuhan Corporation | Active not recruiting | No outcome recorded |
| Phase 4 | NCT07271420 Comparator | Jan 2020 → Dec 2026 expected | end stage renal failure, hypertensive disorder | Chinese University of Hong Kong | Recruiting | No outcome recorded |
| Phase 4 | NCT03640221 Comparator | Sep 2018 → May 2020 | essential hypertension, type 2 diabetes mellitus | Cedars-Sinai Medical Center | Withdrawn | No outcome recorded |
| Phase 4 | NCT03946514 Background | Sep 2018 → Aug 2024 | hypertensive disorder | Shanghai Jiao Tong University School of Medicine | Completed | No outcome recorded |
| Phase 4 | NCT03170336 Comparator | Mar 2018 → Aug 2020 | chronic kidney disease | Guangdong Provincial People's Hospital | Completed | No outcome recorded |
| Phase 4 | NCT04521023 Comparator | Sep 2017 → Jan 2020 | hypertensive disorder | Chong Kun Dang Pharmaceutical | Completed | No outcome recorded |
| Phase 4 | NCT03294070 Background | Sep 2017 → Mar 2018 | hypertensive disorder | Centro Universitario de Ciencias de la Salud, Mexico | Unknown | No outcome recorded |
| Phase 4 | NCT03109795 Comparator | Apr 2017 → Jun 2023 | anxiety, hypertensive disorder | University of Iowa | Terminated | No outcome recorded |
| Phase 4 | NCT03578042 Comparator | Apr 2017 → Sep 2019 | hypertensive disorder | Hotel Dieu de France Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT02774460 Comparator | Feb 2017 → Jun 2021 | hypertensive disorder | Uppsala University | Completed | No outcome recorded |
| Phase 4 | NCT02875886 Comparator | Sep 2016 → Apr 2018 | chronic kidney disease | Erasmus Medical Center | Completed | No outcome recorded |
| Phase 4 | NCT01748123 Comparator | Aug 2016 → Jun 2017 | hypertensive disorder | Johns Hopkins University | Withdrawn | No outcome recorded |
| Phase 4 | NCT02817503 Background | Dec 2015 → Dec 2016 | hyperhomocysteinemia, hypertensive disorder | Second Affiliated Hospital of Nanchang University | Unknown | No outcome recorded |
| Phase 4 | NCT02214498 Comparator | May 2015 → May 2017 | essential hypertension | Erasmus Medical Center | Unknown | No outcome recorded |
| Phase 4 | NCT01922141 Background | May 2015 → Jun 2018 | hypertensive disorder | Novartis Pharmaceuticals | Withdrawn | No outcome recorded |
| Phase 4 | NCT02427880 Background | Apr → Jun 2015 | nephrotic syndrome | Shiraz University of Medical Sciences | Completed | No outcome recorded |
| Phase 4 | NCT02433119 Comparator | Mar 2015 → Sep 2016 | hypertensive disorder | Dong-A ST Co., Ltd. | Completed | No outcome recorded |
| Phase 4 | NCT02373163 Comparator | Sep 2014 → Mar 2016 | hypertensive disorder | Prevencion | Completed | No outcome recorded |
| Phase 4 | NCT01822860 Comparator | Mar 2013 → Feb 2015 | hypertensive disorder | Creighton University | Withdrawn | No outcome recorded |
| Phase 4 | NCT01819441 Background | May 2012 → Dec 2016 | cerebrovascular disorder | Yining Huang | Unknown | No outcome recorded |
| Phase 4 | NCT00987662 Comparator | Jan 2012 → Jan 2013 | hypertensive disorder, obesity disorder | Aristotle University Of Thessaloniki | Withdrawn | No outcome recorded |
| Phase 4 | NCT02046395 Background | Jan 2012 → Dec 2019 | hypertensive disorder, type 2 diabetes mellitus | Tulane University School of Medicine | Completed | No outcome recorded |
| Phase 4 | NCT01519635 Comparator | Oct 2011 → Oct 2014 | hypertensive disorder | Centre Hospitalier Universitaire Vaudois | Completed | No outcome recorded |
| Phase 4 | NCT01030458 Comparator | Sep 2010 → Mar 2012 | hypertensive disorder | KU Leuven | Completed | No outcome recorded |
| Phase 4 | NCT01172431 Comparator | Sep 2010 → Mar 2012 | hypertensive disorder, impaired renal function disease | West China Hospital | Completed | No outcome recorded |
| Phase 4 | NCT01180205 Comparator | Aug 2010 → Oct 2011 | hypertensive disorder | Johannes Gutenberg University Mainz | Unknown | No outcome recorded |
| Phase 4 | NCT01828359 Comparator | Aug 2010 → Jan 2013 | essential hypertension | Hanmi Pharmaceutical Company Limited | Completed | No outcome recorded |
| Phase 4 | NCT01176032 Background | Jun 2010 → Apr 2013 | hypertensive disorder, hypertensive heart disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT01101009 Comparator | Apr 2010 → Nov 2012 | hypertensive disorder | Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company | Completed | No outcome recorded |
| Phase 4 | NCT01271374 Comparator | Apr 2010 → Jun 2011 | hypertensive disorder | InVasc Therapeutics, Inc. | Unknown | No outcome recorded |
| Phase 4 | NCT00438113 Comparator | Dec 2009 → Sep 2016 | atrial fibrillation | Nova Scotia Health Authority | Completed | No outcome recorded |
| Phase 4 | NCT00994253 Comparator | Aug 2009 → Dec 2012 | hypertensive disorder, type 2 diabetes mellitus | Corewell Health East | Withdrawn | No outcome recorded |
| Phase 4 | NCT03115853 Background | Jun 2009 → Jan 2012 | hypertensive disorder | Vanderbilt University Medical Center | Completed | No outcome recorded |
| Phase 4 | NCT00760266 Comparator | Sep 2008 → Apr 2009 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00744237 Comparator | Aug 2008 → Jul 2010 | hypertensive disorder, type 2 diabetes mellitus | Forest Laboratories | Completed | No outcome recorded |
| Phase 4 | NCT00708344 Comparator | Jun 2008 → Jul 2009 | hypertensive disorder | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00673790 Comparator | May 2008 → Jul 2010 | hypertensive disorder | Forest Laboratories | Completed | No outcome recorded |
| Phase 4 | NCT00980187 Comparator | Mar 2008 → Aug 2010 | hypertensive disorder, type 2 diabetes mellitus | LaborMed Pharma S.A. | Completed | No outcome recorded |
| Phase 4 | NCT00605202 Comparator | Feb 2008 → Jan 2009 | potassium deficiency | University of Oulu | Completed | No outcome recorded |
| Phase 4 | NCT01011660 Comparator | Oct 2007 → Aug 2012 | essential hypertension | Chinese Academy of Medical Sciences, Fuwai Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT00745953 Comparator | Aug 2007 → Aug 2009 | metabolic syndrome X | University of Texas Southwestern Medical Center | Withdrawn | No outcome recorded |
| Phase 4 | NCT00500604 Background | Jul 2007 → Jan 2010 | hypertensive disorder | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00509470 Comparator | Jul 2007 → Jun 2012 | essential hypertension | Tokyo University | Completed | No outcome recorded |
| Phase 4 | NCT01375322 Comparator | Jun 2007 → Jun 2010 | hypertensive disorder, proteinuria, type 2 diabetes mellitus | TSH Biopharm Corporation Limited | Completed | No outcome recorded |
| Phase 4 | NCT00887510 Comparator | May 2007 → Nov 2009 | hypertensive disorder | University of Florida | Completed | No outcome recorded |
| Phase 4 | NCT00468923 Comparator | May 2007 → Dec 2015 | stroke disorder | Population Health Research Institute | Completed | No outcome recorded |
| Phase 4 | NCT00775814 Comparator | Oct 2006 → Sep 2008 | hypertensive disorder, obesity disorder | Takeda | Completed | No outcome recorded |
| Phase 4 | NCT00369538 Comparator | Aug 2006 → ? | end stage renal failure, hypertensive disorder, proteinuria | University Hospital, Strasbourg, France | Suspended | No outcome recorded |
| Phase 4 | NCT00362037 Background | Mar 2006 → Jun 2008 | essential hypertension | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00362258 Background | Feb 2006 → Sep 2008 | hypertensive disorder | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00263393 Background | Dec 2005 → Dec 2008 | coronary artery disorder, diabetes mellitus, myocardial infarction, stroke disorder | The George Institute | Completed | No outcome recorded |
| Phase 4 | NCT00277472 Comparator | Nov 2005 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00110422 Comparator | Nov 2005 → Feb 2007 | hypertensive disorder, metabolic syndrome X | Bristol-Myers Squibb | Completed | No outcome recorded |
| Phase 4 | NCT00661895 Background | Aug 2005 → Aug 2009 | hypertensive disorder | Creighton University | Completed | No outcome recorded |
| Phase 4 | NCT00171600 Background | Jul 2005 → Jan 2007 | diabetic kidney disease, hypertensive disorder | Novartis | Terminated | No outcome recorded |
| Phase 4 | NCT00224549 Background | Apr 2005 → Aug 2009 | essential hypertension | Assistance Publique - Hôpitaux de Paris | Completed | No outcome recorded |
| Phase 4 | NCT00171574 Background | Nov 2004 → Jul 2006 | diabetic kidney disease, hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00171132 Background | Aug 2004 → Aug 2007 | hypertensive disorder | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00131846 Comparator | Apr 2004 → Aug 2012 | essential hypertension | Kyoto University | Completed | No outcome recorded |
| Phase 4 | NCT00234858 Comparator | Mar 2004 → Apr 2006 | hypertensive disorder, metabolic syndrome X | Abbott | Completed | No outcome recorded |
| Phase 4 | NCT00232882 Comparator | Dec 2003 → Apr 2006 | essential hypertension | Montreal Clinical Research Institute | Completed | No outcome recorded |
| Phase 4 | NCT00140959 Background | Feb 2003 → Jun 2004 | hypertensive disorder | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00239538 Background | Jan 2003 → Dec 2004 | hypertensive disorder, type 2 diabetes mellitus | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00240474 Background | Dec 2002 → Mar 2004 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00651287 Comparator | Dec 2002 → Jun 2004 | hypertensive disorder | Pfizer | Completed | No outcome recorded |
| Phase 4 | NCT00772499 Comparator | Nov 2002 → Jul 2005 | essential hypertension | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 4 | NCT00274638 Background | Jul 2002 → Jul 2003 | hypertensive disorder | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT03276598 Comparator | Nov 1999 → Apr 2004 | essential hypertension | Helsinki University Central Hospital | Completed | No outcome recorded |
| Phase 4 | NCT00813722 Comparator | Mar 1999 → Jan 2009 | hypertensive disorder | University of Sao Paulo | Unknown | No outcome recorded |
| Phase 4 | NCT00487123 Background | ? → Sep 2007 | essential hypertension | Novartis | Completed | No outcome recorded |
| Phase not applicable23 trials | ||||||
| — | NCT07683585 Comparator | Apr → Jul 2026 overdue | coronary artery disorder, hypertensive disorder | National Medical Research Center for Therapy and Preventive Medicine | Recruiting | No outcome recorded |
| — | NCT07458880 Comparator | Mar 2026 → Sep 2029 expected | intracerebral hemorrhage | The University of Hong Kong | Recruiting | No outcome recorded |
| — | NCT06362668 Comparator | May → Oct 2024 | heart failure | Reprieve Cardiovascular, Inc | Completed | No outcome recorded |
| — | NCT05684055 Comparator | Sep 2023 → May 2025 overdue | hypertensive disorder | University Hospital, Basel, Switzerland | Active not recruiting | No outcome recorded |
| — | NCT03261375 Background | Jan 2021 → Dec 2022 | essential hypertension | Shanghai Golden Leaf MedTec Co. Ltd | Completed | No outcome recorded |
| — | NCT03951558 Comparator | May 2018 → Jun 2019 | idiopathic hypercalciuria, nephrolithiasis | Hospital Infantil de Mexico Federico Gomez | Unknown | No outcome recorded |
| — | NCT03015311 Background | Jan 2017 → Dec 2020 | essential hypertension | Chinese Academy of Medical Sciences, Fuwai Hospital | Unknown | No outcome recorded |
| — | NCT03082742 Comparator | Aug 2015 → Jun 2018 | chronic kidney disease, secondary hyperparathyroidism of renal origin | University of Sao Paulo General Hospital | Unknown | No outcome recorded |
| — | NCT06681116 Comparator | Feb 2015 → Aug 2020 | idiopathic hypercalciuria, nephrolithiasis, calcium oxalate | ALI KAMAL M. SAMI | Completed | No outcome recorded |
| — | NCT02412761 Comparator | Jun 2013 → Jul 2016 | essential hypertension | The University of Texas Health Science Center, Houston | Completed | No outcome recorded |
| — | NCT01996085 Comparator | Jan 2013 → Jun 2016 | hypertensive disorder | Military Institute od Medicine National Research Institute | Completed | No outcome recorded |
| — | NCT01661777 Comparator | Aug 2012 → Aug 2013 | endolymphatic hydrops, eustachian tube disorder | Vanderbilt University | Withdrawn | No outcome recorded |
| — | NCT01425242 Background | Sep 2011 → Dec 2013 | abdominal aortic aneurysm, essential hypertension | Amsterdam UMC, location VUmc | Terminated | No outcome recorded |
| — | NCT01258764 Comparator | Nov 2010 → Mar 2014 | hypertensive disorder | Scripps Translational Science Institute | Completed | No outcome recorded |
| — | NCT00999752 Comparator | Oct 2009 → Feb 2010 | hypertensive disorder | InVasc Therapeutics, Inc. | Completed | No outcome recorded |
| — | NCT00865124 Comparator | Sep 2008 → Aug 2013 | type 2 diabetes mellitus, vascular disorder | Brigham and Women's Hospital | Completed | No outcome recorded |
| — | NCT00478335 Background | May 2007 → Oct 2012 | nephrogenic diabetes insipidus | University of Colorado, Denver | Completed | No outcome recorded |
| — | NCT02336607 Comparator | Dec 2005 → Jun 2006 | hypertensive disorder | AstraZeneca | Completed | No outcome recorded |
| — | NCT00617877 Background | Mar 2005 → Jun 2009 | hypertensive disorder | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| — | NCT00160160 Background | Oct 2004 → ? | hypertensive disorder, type 2 diabetes mellitus | Solvay Pharmaceuticals | Completed | No outcome recorded |
| — | NCT00229242 Comparator | Nov 2003 → Dec 2006 | hypertensive disorder | Queen's University | Completed | No outcome recorded |
| — | NCT00684489 Comparator | Sep 2003 → Mar 2005 | essential hypertension | Medical University of South Carolina | Completed | No outcome recorded |
| — | NCT00214825 Comparator | Aug 2003 → Mar 2006 | diabetes mellitus, proteinuria | Brigham and Women's Hospital | Completed | No outcome recorded |
Press releases naming this drug 3 releases
| Date | Issuer | Release |
|---|---|---|
| 2010-04-07 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces Final Approval of Generic Hyzaar® and Cozaar® tevapharm.com ↗ |
| 2010-03-02 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces Favorable Court Ruling in Generic Hyzaar® and Cozaar® Litigation tevapharm.com ↗ |
| 2006-06-14 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces Tentative Approval of Losartan Potassium & Hydrochlorothiazide Tablets tevapharm.com ↗ |
Evidence & citations 16 cited values
Every value below carries the sentence it was read from. 433 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | hydrochlorothiazide | “This is a phase III, non-inferiority, randomized, double-blind, double-dummy, active-controlled, multicenter study to compare the efficacy and safety of N0877 versus double...” NCT06608472 ↗383“The participant's blood pressure medication regimen will then be altered to initiate a thiazide-type (hydrochlorothiazide or chlorthalidone) or loop diuretic (furosemide,...” NCT04192110 ↗ “OBJECTIVE: To compare the antihypertensive efficacy and safety of once-daily triple therapy with amlodipine (Aml) 10 mg, valsartan (Val) 320 mg, and hydrochlorothiazide (HCTZ)...” PMID 23721363 ↗ Jul 2013 “The purpose of this trial is to evaluate the safety and efficacy of combination therapy of aliskiren/hydrochlorothiazide (HCTZ) 150/25 mg and 300/25 mg compared with HCTZ 25 mg...” NCT00387517 ↗ “Antihypertensive Effects of a Fixed-dose Combination of Losartan and Hydrochlorothiazide Plus Amlodipine Versus a Hydrochlorothiazide and Atenolol Combination Plus Amlodipine...” NCT00140959 ↗ “A Study on the Efficacy and Safety of Olmesartan Medoxomil and Its Combination With Hydrochlorothiazide Compared With an ACE Inhibitor and Its Combination With a Calcium...” NCT00185120 ↗ “Then, losartan 50 mg for 4 weeks, then titrate to losartan 100 mg at Week 4, then titrate to losartan 100 mg + hydrochlorothiazide (HCTZ) 12.5 mg at Week 8, and finally titrate...” NCT00289887 ↗ “Participants will be randomized to one of three first-line antihypertensive agents: (1) the ACE inhibitor perindopril, (2) the AT1 receptor antagonist losartan, or (3) the...” PMID 32039215 ↗ Jan 2020 “COZAAR Plus (Losartan Potassium 50mg/Hydrochlorothiazide 12.5mg) Possibly Titrated up to COZAAR Plus-F (Losartan Potassium 100mg/Hydrochlorothiazide 25mg) in Patients With...” NCT00449111 ↗ “Successful treatment of hypertension accounts for improvements in markers of diastolic function - a pilot study comparing hydrochlorothiazide-based and amlodipine-based...” PMID 19960134 ↗ Dec 2009 “In intervention clusters, lay CHWs independently prescribed and titrated a fixed-dose combination of amlodipine and hydrochlorothiazide, guided by a mobile clinical decision...” PMID 41680483 ↗ Feb 2026 “Two randomized studies were designed to assess the safety, tolerability and efficacy of losartan 100 mg (L100) plus hydrochlorothiazide 12.5 mg (H12.5) in a single fixed-dose...” PMID 24990091 ↗ Jul 2014 “Antihypertensive treatment with low-dose thiazide diuretics at 12.5 mg/day of hydrochlorothiazide or equivalent (Diuretics group) or that without thiazide diuretics...” PMID 25031188 ↗ Jul 2014 “Comparing a Fixed Dose Combination of Telmisartan 80mg Plus Hydrochlorothiazide 12.5mg to Telmisartan 80mg in Patients Who Fail to Respond Adequately to Treatment With Telmisartan 80mg.” NCT00146341 ↗ “This study aimed to evaluate the long-term safety and efficacy of a triple combination therapy with 20 mg azilsartan (AZL), 5 mg amlodipine (AML) and 12.5 mg hydrochlorothiazide (HCTZ).” PMID 29235365 ↗ Dec 2017 “Version 1 contains aspirin 75mg, simvastatin 40mg, Lisinopril 10mg and Atenolol 50mg; Version 2 contains aspirin 75mg, simvastatin 40mg, Lisinopril 10mg and Hydrochlorothiazide 12.5mg.” NCT01057537 ↗ “Version 1 contains aspirin 75mg, simvastatin 40mg, Lisinopril 10mg and Atenolol 50mg; Version 2 contains aspirin 75mg, simvastatin 40mg, Lisinopril 10mg and Hydrochlorothiazide 12.5mg.” NCT01326676 ↗ “4 weeks treatment with candesartan 32 mg (two 16 mg tablets) plus hydrochlorothiazide 25 mg (two 12.5 mg tablets) taken orally with water in the morning between 7 and 10 am.” NCT00867490 ↗ “comparing valsartan monotherapy with valsartan/hydrochlorothiazide (HCTZ) combination therapy as initial treatment for high-risk patients with stage 2 hypertension” PMID 18498915 ↗ Apr 2008 “Other drugs, including CCB (amlodipine preferred), diuretics (hydrochlorothiazide preferred), and β-blockers, are allowed, in order to achieve the SBP target.” NCT02817503 ↗ “run-in treatment period with telmisartan 80 mg plus hydrochlorothiazide 12.5 mg (T80/H12.5) taken as a single tablet once per day for approximately six weeks.” NCT00239369 ↗ “A combination tablet containing Aspirin 81 mg, enalapril 5 mg (or valsartan 40 mg), atorvastatin 20 mg and hydrochlorothiazide 12.5 mg taken once daily” NCT01271985 ↗ “Japanese patients with uncontrolled essential hypertension received single-blind losartan 50 mg/hydrochlorothiazide 12.5 mg (L50/H12.5) for 8 weeks.” PMID 25271811 ↗ Oct 2014 “Decongestive therapy with e.v. furosemide +/- hydrochlorothiazide will be adjusted by intraabdominal pressure and/or point of care ultrasound” NCT07008365 ↗ “A capsule of Polycap ® contains 100mg of Aspirin, 20mg of simvastatin, 12.5mg hydrochlorothiazide, 5mg of ramipril and 50mg of atenolol.” NCT05963568 ↗ “The trial compared a Polypill (75 mg aspirin, 20 mg simvastatin, 10 mg lisinopril and 12.5 mg hydrochlorothiazide) to Standard Practice.” PMID 21205325 ↗ Jan 2011 “polypill (containing 40 mg of simvastatin, 100 mg of atenolol, 25 mg of hydrochlorothiazide, and 10 mg of ramipril) or placebo daily” PMID 33186492 ↗ Nov 2020 “The mainstays of management of endolymphatic hydrops are a low sodium diet and diuretic treatment (hydrochlorothiazide/triamterene).” NCT01661777 ↗ “The polypill comprises hydrochlorothiazide 12.5 mg, aspirin 81 mg, atorvastatin 20 mg, and either enalapril 5 mg or valsartan 40 mg.” PMID 32894967 ↗ Aug 2020 “A capsule of Polycap contained aspirin 100 mg, simvastatin 20 mg, hydrochlorothiazide 12.5 mg, ramipril 5 mg, and atenolol 50 mg.” PMID 39082406 ↗ Jul 2024 “the cardiovascular polypill (aspirin 75 mg, simvastatin 40 mg, lisinopril 10 mg, and hydrochlorothiazide 12.5 mg) in the evening” PMID 23382539 ↗ Feb 2013 “The amlodipine/benazepril and benazepril/hydrochlorothiazide dual therapies were comparable in ambulatory systolic BP lowering.” PMID 38263021 ↗ Jan 2024 “Candesartan/Hydrochlorothiazide(Candemore Plus® Tab) Versus Candesartan/Amlodipine(Cantabell® Tab) in Hypertensive Patients” NCT04521023 ↗ “Fixed dose combination therapy - aspirin 81mg, hydrochlorothiazide 12.5mg, enalapril 2.5mg and atorvastatin 20mg Once daily” NCT00603590 ↗ “Drugs used were hypertension medications were: chlorothiazide, hydrochlorothiazide, polythiazide indapamide, metolazone” NCT00684489 ↗ “comparing hydrochlorothiazide 25-50 mg, amiloride 10-20 mg and combination of both diuretics at half these doses.” PMID 26253567 ↗ Aug 2015 “Each pill contains acetylsalicylic acid 81 mg, atorvastatin 20 mg, hydrochlorothiazide 12.5 mg, valsartan 40 mg” NCT01245608 ↗ “hydrochlorothiazide (HCTZ) is a drug indicated for the treatment of patients with mild to moderate hypertension” NCT01294631 ↗ “Coated, Oral tablet containing Olmesartan medoxomil(OM)-Hydrochlorothiazide(HCTZ) 20-12.5mg, given once a day.” NCT01838850 ↗ “One hydrochlorothiazide 12.5 mg tablet + one hydrochlorothiazide 12.5 mg placebo tablet taken once per day.” NCT00923091 ↗ “Other drugs, including hydrochlorothiazide and β-blockers, are allowed, in order to achieve the SBP target.” NCT03015311 ↗ “valsartan 160 mg once a day for 6 months plus hydrochlorothiazide 25 mg a tablet once a day for 6 months” NCT00687206 ↗ “Atenolol 100 mg for 4 weeks followed by atenolol 100 mg + hydrochlorothiazide 12.5 mg for 4 weeks” NCT00232882 ↗ “Treatment with irbesartan 300mg for 4 weeks. IF ABP\>135/85 mmHg add hydrochlorothiazide 12.5 mg.” NCT00987662 ↗ “After 4 weeks of titration, hydrochlorothiazide 12.5 mg could be optionally added to both groups.” PMID 22035131 ↗ Oct 2011 “Hydrochlorothiazide, metolazone, chlorthalidone, chlorothiazide, bendroflumethiazide, indapamide” NCT04330300 ↗ “Polipill version 2: aspirin 75mg, simvastatin 40mg, lisinopril 10mg, hydrochlorothiazide 12.5mg.” NCT01313702 ↗ “single-pill combination of the direct renin inhibitor aliskiren and hydrochlorothiazide (HCT)” PMID 19203020 ↗ Dec 2008 “candesartan at a dose of 16 mg per day plus hydrochlorothiazide at a dose of 12.5 mg per day” PMID 27041480 ↗ Apr 2016 “Tablet containing losartan potassium (100 mg) and hydrochlorothiazide (12.5 mg), once daily” NCT01307046 ↗ “Telmisartan 80 mg/Amlodipine 5 mg/Hydrochlorothiazide 12.5 mg Fixed-dose Combination Tablet” NCT02183675 ↗ “Encapsulated Hydrochlorothiazide 12.5 mg or 25 mg total daily dosage, oral administration” NCT00673790 ↗ “Thereafter addition of semaglutide, pentoxifylline, hydrochlorothiazide, and baricitinib.” NCT05897372 ↗ “either a combined pill of ACE inhibitors and diuretics (Hydrochlorothiazide/Lisinopril)” NCT05049616 ↗ “Step IV: olmesartan 20 mg or 40 mg + amlodipine 10 mg + hydrochlorothiazide 12.5 mg” NCT03024476 ↗ “Step 2: Combination drug containing losartan 50 mg and hydrochlorothiazide 12.5 mg” NCT01198496 ↗ “Olmesartanmedoxomil (OM) /Hydrochlorothiazide (HCTZ)40/12.5 mg tablets once daily” NCT00441350 ↗ “Valsartan 160mg and Hydrochlorothiazide 12.5mg, tablet, once a day for 8 weeks” NCT02433119 ↗ “telmisartan 80 mg + hydrochlorothiazide (HCTZ) 12.5 mg fixed dose combination” NCT01911780 ↗ “one 12.5 mg hydrochlorothiazide (HCTZ) tablet daily, orally, for 12 weeks.” NCT00806585 ↗ “once daily Telmisartan 80 mg/Hydrochlorothiazide 12.5 mg (Micardis Plus)” NCT00257491 ↗ “Step 2 - combination of Accupril with Hydrochlorothiazide 12.5 mg po od.” NCT00438113 ↗ “hydrochlorothiazide and angiotensin receptor blocker (valsartan) therapy” PMID 20498618 ↗ Aug 2010 “combination valsartan/hydrochlorothiazide (HCTZ) vs. amlodipine/HCTZ” PMID 21974760 ↗ Jul 2011 “Fixed dose Combination of Fimasartan/Amlodipine/Hydrochlorothiazide” NCT03629067 ↗ “500 mg BID + hydrochlorothiazide (HCTZ) 25 mg once daily \[QD\]” NCT03198793 ↗ “amlodipine 10mg + irbesartan 300mg + hydrochlorothiazide 12.5mg” NCT06790927 ↗ “Losartan 50 mg / Hydrochlorothiazide (HCTZ) 12.5 mg Combination” NCT01431508 ↗ “Fimasartan/Hydrochlorothiazide combination 60/12.5mg 120/12.5mg” NCT01258673 ↗ “amiloride/hydrochlorothiazide 1.25-2.5 mg/12.5-25 mg (Group A)” PMID 22329591 ↗ Apr 2012 “CoAprovel (300/12.5mg hydrochlorothiazide one per day per os.” NCT00362037 ↗ “irbesartanhydrochlorothiazide 162.5 mg/d, amlodipine 5 mg/d” NCT03660397 ↗ “valsartan/hydrochlorothiazide (HCTZ) combination therapy” NCT00698646 ↗ “160+12,5 mg valsartan+hydrochlorothiazide combination” NCT01425411 ↗ “Hydrochlorothiazide 12.5 mg p.o. tablet once daily” NCT01425242 ↗ “CoAprovel (300/12.5mg hydrochlorothiazide)” NCT00362258 ↗ “CoAprovel (300/12.5mg hydrochlorothiazide)” NCT00335673 ↗ “Telmisartan / Hydrochlorothiazide (HCTZ)” NCT02262780 ↗ “hydrochlorothiazide 25 mg/day (ESIDREX®)” NCT02824718 ↗ “Hydrochlorothiazide (25 mg) Monotherapy” NCT00277472 ↗ “hydrochlorothiazide (HCT G.L) 25mg” NCT06710600 ↗ “Nifedipine + hydrochlorothiazide” NCT03261375 ↗ “hydrochlorothiazide [thiazide]” PMID 37039792 ↗ Apr 2023 “Hydrochlorothiazide (HCTZ)” NCT01302899 ↗ “Hydrochlorothiazide (HCTZ)” NCT01113047 ↗ “Hydrochlorothiazide (HCTZ)” NCT01259297 ↗ “Drug: Hydrochlorothiazide” NCT01180205 ↗ “HCTZ-hydrochlorothiazide” NCT00574834 ↗ “Hydrochlorothiazide25mg” NCT00926289 ↗ “Hydrochlorothiazide” NCT00459056 ↗ “hydrochlorothiazide” NCT02765009 ↗ |
| Known as | Diazide | “Diazide” NCT00621153 ↗ |
| Known as | Dichlozid | “Dichlozid 1 Tab.(Hydrochlorothiazide 25.0 mg) would be administered orally once” NCT02739672 ↗1“Dichlozid 1 Tab.(Hydrochlorothiazide 12.5 mg) would be administered orally once” NCT03032315 ↗ |
| Known as | Dichlozid Tab | “Dichlozid Tab® (hydrochlorothiazide 25 mg)” NCT00496834 ↗ |
| Known as | H12.5 | “50 mg losartan potassium (L50), 12.5 mg hydrochlorothiazide (H12.5), and 5 mg amlodipine besylate (A5)” NCT01302691 ↗ |
| Known as | HCT | “The majority of patients with essential hypertension of moderate severity (WHO grade 2) require combination therapy. We aimed to investigate whether the single-pill combination...” PMID 21117946 ↗ Nov 20106“Angiotensin-converting enzyme inhibitors combined with higher doses of hydrochlorothiazide (HCT), that is, 25 mg daily, have been recognized as an effective form of...” PMID 18463672 ↗ May 2008 “PURPOSE: To investigate the pharmacokinetic/pharmacodynamic (PK/PD) interaction between irbesartan (IRB) and hydrochlorothiazide (HCT) in normotensive subjects.” PMID 25545238 ↗ Feb 2015 “At visit 4, if the patients did not achieve BP goal, HCT 12.5 mg/day was added to Aliskiren/Amlodipine/HCT (300/10/12.5 mg/day) for 4 weeks.” NCT01070030 ↗ “single-pill combination of the direct renin inhibitor aliskiren and hydrochlorothiazide (HCT)” PMID 19203020 ↗ Dec 2008 “Hydrochlorothiazide (HCT)” NCT07593612 ↗ “Hydrochlorothiazide (HCT)” NCT00775814 ↗ |
| Known as | HCT G.L | “hydrochlorothiazide (HCT G.L) 25mg” NCT06710600 ↗ |
| Known as | HCTZ | “The general aim and clinical objective of this trial is to determine the effect of telmisartan 80 mg compared to losartan 50 mg + HCTZ (Hydrochlorothiazide) 12.5 mg on...” NCT02183701 ↗108“OBJECTIVE: The aim of this study was to determine whether a triple combination of olmesartan medoxomil (OM), amlodipine besylate (AML), and hydrochlorothiazide (HCTZ) had a...” PMID 20678674 ↗ Jul 2010 “The purpose of this trial is to evaluate the safety and efficacy of combination therapy of aliskiren/hydrochlorothiazide (HCTZ) 150/25 mg and 300/25 mg compared with HCTZ 25 mg...” NCT00387517 ↗ “The authors examined effects of valsartan and hydrochlorothiazide (HCTZ) combined and alone on insulin sensitivity (using homeostasis model assessment-insulin resistance...” PMID 19120715 ↗ Dec 2008 “In patients with acute heart failure, the addition of hydrochlorothiazide (HCTZ) to furosemide increased the diuretic response in the CLOROTIC trial (Combining Loop with...” PMID 40590131 ↗ Jul 2025 “Then, losartan 50 mg for 4 weeks, then titrate to losartan 100 mg at Week 4, then titrate to losartan 100 mg + hydrochlorothiazide (HCTZ) 12.5 mg at Week 8, and finally titrate...” NCT00289887 ↗ “This 28- to 54-week, open-label, multicenter study evaluated the safety and efficacy of a triple combination, aliskiren with amlodipine and hydrochlorothiazide (HCTZ), in...” PMID 23205748 ↗ Aug 2012 “Olmesartan medoxomil was uptitrated to 40 mg/day (weeks 4-6), then olmesartan medoxomil/hydrochlorothiazide (HCTZ) 40/12.5 mg per day (weeks 7-9), and olmesartan medoxomil/HCTZ...” PMID 20653330 ↗ 2010 “The impact of an ARB, with or without hydrochlorothiazide (HCTZ), on glycaemic factors and the risk for developing diabetes in hypertensive patients with the metabolic syndrome...” PMID 20147971 ↗ Feb 2010 “An eight week study to compare the effect of a fixed dose combination of Telmisartan 40 mg plus hydrochlorothiazide (HCTZ) 12.5 mg to Telmisartan 40 mg alone on diastolic and...” NCT02177500 ↗ “Hydrochlorothiazide (HCTZ) ATC class: C03AA03 Form: Tablet Dose range: Phase 1: 25mg (2 x 12.5mg tablet) Phase 2: 50mg (4 x 12.5mg tablet) Maximum allowed dose: 50mg...” NCT02351973 ↗ “This study aimed to evaluate the long-term safety and efficacy of a triple combination therapy with 20 mg azilsartan (AZL), 5 mg amlodipine (AML) and 12.5 mg hydrochlorothiazide (HCTZ).” PMID 29235365 ↗ Dec 2017 “The antihypertensive efficacy and tolerability of losartan (LST) in fixed combination with hydrochlorothiazide (HCTZ) has not been compared to those of amlodipine monotherapy in Asians.” PMID 19949604 ↗ Apr 2009 “the blood pressure (BP)-lowering efficacy and safety of an olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ)-based titration regimen in patients aged ≥65 years with hypertension.” PMID 21639407 ↗ Jun 2011 “This non-randomized study investigated whether valsartan 160 mg/hydrochlorothiazide 25 mg (Val 160/HCTZ 25) in fixed dose combination could provide additional blood pressure control” PMID 17922981 ↗ Nov 2007 “Thiazide doses equivalent to 1 to 2 mg/kg/d of hydrochlorothiazide (HCTZ) have been proposed to correct hypercalciuria and prevent kidney failure in patients with Dent disease.” PMID 18976849 ↗ Oct 2008 “comparing valsartan monotherapy with valsartan/hydrochlorothiazide (HCTZ) combination therapy as initial treatment for high-risk patients with stage 2 hypertension” PMID 18498915 ↗ Apr 2008 “Optional add-on of hydrochlorothiazide (HCTZ) (12.5-25 mg) was allowed (as applicable per local country regulations) for adequate blood pressure control.” NCT01256411 ↗ “We performed 12-hour urine collections in 7 patients taking 25 mg of chlorthalidone (CTD) and 10 patients taking 25 mg of hydrochlorothiazide (HCTZ).” PMID 40194294 ↗ Apr 2025 “Study to Evaluate the Efficacy and Safety of Aliskiren Hydrochlorothiazide (HCTZ) vs Ramipril in Obese patients (BMI ≥ 30) with Stage 2 Hypertension” NCT00772577 ↗ “Both Olmesartan (OLM)/Amlodipine (AML) combination and Hydrochlorothiazide (HCTZ) have proven to be efficacious and safe in lowering blood pressure” NCT00902538 ↗ “This study investigated potential pharmacokinetic drug-drug interactions between empagliflozin and hydrochlorothiazide (HCTZ) or torasemide (TOR).” PMID 25636696 ↗ Jan 2015 “olmesartan medoxomil (OM) /hydrochlorothiazide (HCTZ) tablets 40mg/25mg + 20mg/12.5mg matching placebo tablet once daily for 8 weeks” NCT00430508 ↗ “Optional addition of Hydrochlorothiazide (HCTZ)of 12.5 mg with increase to 25 mg was allowed for patients not adequately controlled.” NCT00402103 ↗ “Antihypertensive efficacy and safety of losartan/hydrochlorothiazide (HCTZ) combinations have not been adequately studied in Asians.” PMID 19390542 ↗ Apr 2009 “losartan potassium 50 mg/12.5 Hydrochlorothiazide (HCTZ) titrated as needed to losartan potassium 100 mg/25 mg Hydrochlorothiazide” NCT00546754 ↗ “Patients will be given Losartan LS (50 mg per day) and Hydrochlorothiazide (HCTZ) 12.5 mg per day as a combination therapy.” NCT06491940 ↗ “Hydrochlorothiazide (HCTZ) 12.5 mg for week 1; Hydrochlorothiazide (HCTZ) 25 mg (with or without amlodipine)for 7 weeks” NCT00760266 ↗ “Benazepril hydrochloride (HCl)/hydrochlorothiazide (HCTZ) 20/12.5 mg capsules for oral administration once daily.” NCT00170950 ↗ “This study will give the patients nebivolol or hydrochlorothiazide (HCTZ) for 6 weeks after 2 weeks of placebo.” NCT02710071 ↗ “hydrochlorothiazide (HCTZ) is a drug indicated for the treatment of patients with mild to moderate hypertension” NCT01294631 ↗ “Coated, Oral tablet containing Olmesartan medoxomil(OM)-Hydrochlorothiazide(HCTZ) 20-12.5mg, given once a day.” NCT01838850 ↗ “olmesartan medoxomil plus hydrochlorothiazide (HCTZ) in patients with hypertension and type 2 diabetes” PMID 21777013 ↗ Sep 2011 “the investigator will have the option, according to his clinical criteria, to add 12.5 mg of HCTZ QD” NCT03294070 ↗ “valsartan/hydrochlorothiazide 160/25 (Fixed Dose Combination of Valsartan 160 mg Plus HCTZ 25 mg)” NCT00171015 ↗ “hydrochlorothiazide (HCTZ) + potassium, 12.5 mg/10 milliequivalents (mEq) capsule daily” NCT00865124 ↗ “Hydrochlorothiazide (HCTZ) 12.5 mg tablets taken once a day during the Extension Phase.” NCT00523744 ↗ “Olmesartanmedoxomil (OM) /Hydrochlorothiazide (HCTZ)40/12.5 mg tablets once daily” NCT00441350 ↗ “amlodipine (AML)/olmesartan medoxomil (OM)±hydrochlorothiazide (HCTZ) algorithm” PMID 23254596 ↗ Dec 2012 “telmisartan 80 mg + hydrochlorothiazide (HCTZ) 12.5 mg fixed dose combination” NCT01911780 ↗ “one 12.5 mg hydrochlorothiazide (HCTZ) tablet daily, orally, for 12 weeks.” NCT00806585 ↗ “60 mg FMS + 12.5 mg hydrochlorothiazide (HCTZ) once a day during 4 weeks.” NCT02466490 ↗ “then crossed over to hydrochlorothiazide (HCTZ) once daily for 2 weeks” NCT02412761 ↗ “hydrochlorothiazide (HCTZ) 25mg OD, increased to 50 mg OD at 3 weeks.” NCT00834600 ↗ “combination valsartan/hydrochlorothiazide (HCTZ) vs. amlodipine/HCTZ” PMID 21974760 ↗ Jul 2011 “Chlorthalidone (CTD) may be superior to hydrochlorothiazide (HCTZ)” PMID 36067089 ↗ Sep 2022 “Losartan 50 mg / Hydrochlorothiazide (HCTZ) 12.5 mg Combination” NCT01431508 ↗ “Telmisartan / Hydrochlorothiazide (HCTZ) Fixed Dose Combination” NCT02187523 ↗ “500 mg BID + hydrochlorothiazide (HCTZ) 25 mg once daily \[QD\]” NCT03198793 ↗ “Hydrochlorothiazide (HCTZ) is a common anti-hypertensive drug.” PMID 38828023 ↗ May 2024 “olmesartan medoxomil (OM)+ hydrochlorothiazide (HCTZ) tablets” NCT00430950 ↗ “hydrochlorothiazide (HCTZ; n=104) or azelnidipine (n=103)” PMID 21241987 ↗ Dec 2010 “Valsartan and hydrochlorothiazide (HCTZ) - monotherapy” NCT00902304 ↗ “Verapamil SR/Trandolapril/Hydrochlorothiazide (HCTZ)” NCT00133692 ↗ “Aliskiren/Amlodipine and Hydrochlorothiazide (HCTZ)” NCT00942994 ↗ “losartan 50 mg/hydrochlorothiazide (HCTZ) 12.5 mg” NCT00447603 ↗ “the thiazide diuretic hydrochlorothiazide (HCTZ)” PMID 32039215 ↗ Jan 2020 “combination valsartan/hydrochlorothiazide (HCTZ)” PMID 20010618 ↗ Dec 2009 “Aliskiren/hydrochlorothiazide (HCTZ) (300/25 mg)” NCT00705575 ↗ “telmisartan 80 mg and HCTZ (Hydrochlorothiazide)” NCT02177422 ↗ “hydrochlorothiazide (HCTZ) 25 mg for 9 days” NCT01198249 ↗ “Hydrochlorothiazide (HCTZ) 25 milligrams.” NCT07469722 ↗ “Hydrochlorothiazide (HCTZ) 25 milligrams.” NCT07687160 ↗ “multiple-dose hydrochlorothiazide (HCTZ)” NCT03387657 ↗ “Hydrochlorothiazide (HCTZ) 12.5-25 mg” NCT00386607 ↗ “Valsartan/hydrochlorothiazide (HCTZ)” NCT00548067 ↗ “hydrochlorothiazide (HCTZ) 25 mg/day” PMID 28509725 ↗ Oct 2017 “hydrochlorothiazide (HCTZ) 12.5 mg” NCT00240474 ↗ “hydrochlorothiazide (HCTZ) 12.5 mg” NCT02177435 ↗ “hydrochlorothiazide (HCTZ) 6.25 mg” NCT00153049 ↗ “hydrochlorothiazide (HCTZ) 12.5 mg” NCT01975246 ↗ “Hydrochlorothiazide (HCTZ))” NCT00396656 ↗ “Losartan 100mg/ HCTZ 12.5mg” NCT01828359 ↗ “Hydrochlorothiazide (HCTZ)” NCT02183675 ↗ “Hydrochlorothiazide (HCTZ)” NCT00765674 ↗ “Hydrochlorothiazide (HCTZ)” NCT01302899 ↗ “hydrochlorothiazide (HCTZ)” PMID 18593517 ↗ Jun 2008 “Hydrochlorothiazide (HCTZ)” NCT06681116 ↗ “Hydrochlorothiazide (HCTZ)” NCT01370655 ↗ “hydrochlorothiazide (HCTZ)” NCT00496834 ↗ “Hydrochlorothiazide (HCTZ)” NCT02072330 ↗ “Hydrochlorothiazide (HCTZ)” NCT01113047 ↗ “Hydrochlorothiazide (HCTZ)” NCT02185417 ↗ “Hydrochlorothiazide (HCTZ)” NCT02276378 ↗ “Hydrochlorothiazide (HCTZ)” NCT01259297 ↗ “Hydrochlorothiazide (HCTZ)” NCT00671424 ↗ “Hydrochlorothiazide (HCTZ)” NCT00787605 ↗ “HCTZ-hydrochlorothiazide” NCT00574834 ↗ “HCTZ 12.5 mg capsule.” NCT00698646 ↗ “HCTZ” NCT00621153 ↗ |
| Known as | HTC | “administration of hydrochlorothiazide (HTC) once daily for 4 days (10 patients)” NCT01276288 ↗ |
| Known as | Hydrochlorothiazid | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01879527 ↗ |
| Known as | hydrochlorothiazide 25 milligrams | “hydrochlorothiazide 25 milligrams” NCT07008365 ↗ |
| Known as | Hydrochlorthiazide | “Hydrochlorthiazide® (Hydrochlorothiazide)” NCT02774460 ↗ |
| Known as | Hyzaar | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01620788 ↗ |
| Known as | Thiazide | ClinicalTrials.gov intervention name — accepted as the source's own label NCT00232882 ↗ |
| Action | Inhibit | “Na-Cl co-transporter activity is inhibited by thiazides.” PMID 20555294 ↗ Aug 2010 |
| Route | Oral | “Tablets, Oral” NCT00095394 ↗ |