Drugs / Citalopram
last change Jun 2026 re-read 2 minutes ago

Citalopram

Small molecule

Developed for
depressive disorder · major depressive disorder · acute coronary syndrome · Alzheimer disease · anxiety · dementia · schizophrenia · stroke disorder
+35 more · autism spectrum disorder · cocaine dependence · gastroesophageal reflux disease · obsessive-compulsive disorder · Parkinson disease · traumatic brain injury · alcohol abuse · alcohol dependence · asthma · autism · bipolar disorder · circadian rhythm sleep disorder, delayed sleep phase type · cocaine abuse · dysthymic disorder · fibromyalgia · Friedreich ataxia · frontotemporal dementia · Huntington disease · irritable bowel syndrome · myalgic encephalomeyelitis/chronic fatigue syndrome · panic disorder · prurigo nodularis · rheumatoid arthritis · schizophreniform disorder · vascular dementia · bipolar depression · borderline personality disorder · burning mouth syndrome · ischemic stroke · mood disorder · myocardial infarction · myofascial pain syndrome · neurotic depression · premature ejaculation · temporomandibular joint disorder
Investigated by
National Institute of Mental Health (NIMH) · University of Oxford · National Heart, Lung, and Blood Institute (NHLBI) · New York State Psychiatric Institute · University of Pittsburgh · Actavis Inc.
+138 more · National Institute on Drug Abuse (NIDA) · Sunnybrook Health Sciences Centre · University of Michigan · Centre for Addiction and Mental Health · Columbia University · Emory University · Indiana University · Massachusetts General Hospital · Mayo Clinic · National Institute of Mental Health and Neuro Sciences, India · National Institute on Aging (NIA) · Ontario Mental Health Foundation · Stanford University · The University of Texas Health Science Center, Houston · Torrent Pharmaceuticals Limited · Universitaire Ziekenhuizen KU Leuven · University of Bath · University of North Carolina, Chapel Hill · 59th Medical Wing · Alliance for Clinical Trials in Oncology · Alzheimer Society of Canada · Amsterdam UMC, location VUmc · Artesis University College, Antwerp · Asthma UK · Big Health Inc. · Boehringer Ingelheim · Boston University · Bruce Pollock · CIHR Canadian HIV Trials Network · California Pacific Medical Center Research Institute · Canadian Institutes of Health Research (CIHR) · Capital Medical University · Catalan Institute of Oncology · Central Hospital, Nancy, France · Centre Hospitalier Universitaire Vaudois · Centre de Recherche du Centre Hospitalier de l'Université de Montréal · Chang Gung Memorial Hospital · Charite University, Berlin, Germany · Chih-Wei Tang · Ciusss de L'Est de l'Île de Montréal · Cure Huntington's Disease Initiative (CHDI) · Dalian Seventh People's Hospital · Danish University Antidepressant Group · Demensforbundet, Norway · Ege University · First Hospital of China Medical University · French National Institute of Health and Medical Research · German Research Foundation · Gitte Moos Knudsen · Hadassah Medical Organization · Hamilton Health Sciences Corporation · Hannover Medical School · Henry Ford Health System · HolsboerMaschmeyer NeuroChemie GmbH · Hospices Civils de Lyon · Hospital Regional 1o de Octubre · Hospital Universitari de Bellvitge · Hunter Holmes McGuire VA Medical Center · Idorsia Pharmaceuticals Ltd. · Innlandet Hospital Trust · Irish Cancer Society · JHSPH Center for Clinical Trials · James A. Haley Veterans Administration Hospital · Jing-Ho Mental Hospital, Taiwan · John V. Campo, M.D. · Johnson & Johnson Pharmaceutical Research & Development, L.L.C. · King's College London · Liam Heaney · Marina Klein · Max-Planck-Institute of Psychiatry · McMaster University · Mclean Hospital · Medical University of Vienna · Medtronic - MITG · all 144 on the full record

Regulatory milestones approvals, filings & regulatory actions · 1 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Approved US (FDA) CELEXA 1998-07-17 fda.gov

Trials 100 · started per year

today
US approved 1998
1
1
1
1
5
2
7
6
7
6
2
1
5
8
3
3
4
6
4
1
2
4
6
6
1
1
2
1
1995199619971998199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020212022202320242025202620272028
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 02 trials
Phase 0 NCT06796946 Jun → Dec 2026 expected University of Huelva Not yet recruiting No outcome recorded
Phase 0 NCT02269540 Oct 2014 → Jun 2018 major depressive disorder Centre for Addiction and Mental Health Completed No outcome recorded
Phase 114 trials
Phase 1 NCT04097288 Sep 2019 → Feb 2020 female stress incontinence University Hospital Bispebjerg and Frederiksberg Completed No outcome recorded
Phase 1 NCT03907215 Apr → Jun 2019 Idorsia Pharmaceuticals Ltd. Completed No outcome recorded
Phase 1 NCT03854578 Mar → Aug 2019 major depressive disorder Boehringer Ingelheim Completed No outcome recorded
Phase 1 NCT02092974 Apr → Dec 2014 Charite University, Berlin, Germany Completed No outcome recorded
Phase 1 NCT01978782 Jan → Apr 2014 HIV infectious disease, depressive disorder Radboud University Medical Center Completed No outcome recorded
Phase 1 NCT01951053 Jan → May 2010 Johnson & Johnson Pharmaceutical Research & Development, L.L.C. Completed No outcome recorded
Phase 1 NCT00538889 Aug → Nov 2007 Wyeth is now a wholly owned subsidiary of Pfizer Completed No outcome recorded
Phase 1 NCT00609531 Jan 2007 → Aug 2009 autism spectrum disorder University of North Carolina, Chapel Hill Completed No outcome recorded
Phase 1 NCT00613470 Mar 2005 → May 2013 depressive disorder Mayo Clinic Completed No outcome recorded
Phase 1 NCT00865943 Jul → Aug 2003 Actavis Inc. Completed No outcome recorded
Phase 1/23 trials
Phase 1/2 NCT06017037 May 2023 → May 2024 atypical depressive disorder University of Oxford Unknown No outcome recorded
Phase 1/2 NCT01667744 Jan → Feb 2016 acute coronary syndrome Henry Ford Health System Withdrawn No outcome recorded
Phase 1/2 NCT01032018 Jan 2010 → Jan 2012 acute coronary syndrome, depressive disorder Columbia University Completed No outcome recorded
Phase 217 trials
Phase 2 NCT05063604 May 2022 breast cancer, major depressive disorder Hospital Universitari de Bellvitge Terminated No outcome recorded
Phase 2 NCT04766229 Jun 2021 → Nov 2022 cancer, insomnia University College Dublin Completed No outcome recorded
Phase 2 NCT04497168 Apr 2021 → Mar 2026 Parkinson disease University of Michigan Completed No outcome recorded
Phase 2 NCT03222570 Feb 2018 → Apr 2024 depressive disorder University of Minnesota Completed No outcome recorded
Phase 2 NCT03899285 Jan → Dec 2018 major depressive disorder Ciusss de L'Est de l'Île de Montréal Completed No outcome recorded
Phase 2 NCT02458690 Jul 2015 → Aug 2019 coronary artery disorder, dysthymic disorder, major depressive disorder, stroke disorder Indiana University Completed No outcome recorded
Phase 2 NCT02113943 Apr → Jun 2014 French National Institute of Health and Medical Research Completed No outcome recorded
Phase 2 NCT02000726 Jul 2013 → Jun 2014 depressive disorder University of Michigan Withdrawn No outcome recorded
Phase 2 NCT02080832 Feb 2010 → Feb 2016 cocaine dependence Virginia Commonwealth University Completed No outcome recorded
Phase 2 NCT00742573 Aug 2008 → Jan 2014 major depressive disorder New York State Psychiatric Institute Completed No outcome recorded
Phase 2/33 trials
Phase 2/3 NCT00962039 Jul 2004 → Apr 2010 anxiety John V. Campo, M.D. Completed No outcome recorded
Phase 2/3 NCT00080158 Mar 2004 → Jun 2007 depressive disorder New York State Psychiatric Institute Completed No outcome recorded
Phase 2/3 NCT00018902 Jan 2001 → Mar 2007 depressive disorder University of Pittsburgh Completed No outcome recorded
Phase 39 trials
Phase 3 NCT05041582 Sep 2021 → Aug 2024 stroke disorder Chih-Wei Tang Unknown No outcome recorded
Phase 3 NCT02374567 Jan 2015 → Jun 2017 anxiety disorder, dementia, depressive disorder, schizophrenia +1 Hannover Medical School Terminated No outcome recorded
Phase 3 NCT00898807 Jul 2009 → Sep 2013 Alzheimer disease JHSPH Center for Clinical Trials Completed No outcome recorded
Phase 3 NCT00317746 Nov 2006 → Mar 2012 HIV infectious disease, depressive disorder, hepatitis C virus infection Marina Klein Completed No outcome recorded
Phase 3 NCT00363909 Nov 2006 → Jun 2007 breast cancer Alliance for Clinical Trials in Oncology Completed No outcome recorded
Phase 3 NCT00361218 Oct 2005 → Dec 2008 major depressive disorder Massachusetts General Hospital Completed No outcome recorded
Phase 3 NCT00249886 Sep 2002 → Nov 2006 major depressive disorder Sunnybrook Health Sciences Centre Withdrawn No outcome recorded
Phase 3 NCT00000368 Feb 1999 → Jul 2004 agoraphobia, panic disorder New York State Psychiatric Institute Completed No outcome recorded
Phase 3 NCT00009204 Sep 1995 → Apr 2000 Alzheimer disease, vascular dementia Bruce Pollock Completed No outcome recorded
Phase 424 trials
Phase 4 NCT03499171 May 2019 → Apr 2021 gastroesophageal reflux disease Universitaire Ziekenhuizen KU Leuven Unknown No outcome recorded
Phase 4 NCT03993535 Oct 2018 → Apr 2023 obsessive-compulsive disorder University of Sao Paulo Completed No outcome recorded
Phase 4 NCT03746691 Feb → Jul 2017 gastroesophageal reflux disease Universitaire Ziekenhuizen KU Leuven Completed No outcome recorded
Phase 4 NCT02711215 May 2015 → Jan 2020 major depressive disorder Medical University of Vienna Unknown No outcome recorded
Phase 4 NCT02473250 Jan 2015 → Dec 2019 bipolar disorder New York State Psychiatric Institute Completed No outcome recorded
Phase 4 NCT01916824 Aug 2013 → Dec 2015 major depressive disorder Emory University Completed No outcome recorded
Phase 4 NCT01716221 Oct 2012 → Mar 2013 Friedreich ataxia University of Colorado, Denver Completed No outcome recorded
Phase 4 NCT01796132 Aug 2012 → Dec 2016 depressive disorder, lactation disease Centre Hospitalier Universitaire Vaudois Unknown No outcome recorded
Phase 4 NCT01557946 Mar 2012 → Sep 2015 major depressive disorder Mclean Hospital Completed No outcome recorded
Phase 4 NCT01436643 Nov 2011 → Sep 2013 depressive disorder, relapsing-remitting multiple sclerosis Novartis Pharmaceuticals Terminated No outcome recorded
Phase not applicable28 trials
NCT06949644 Sep 2025 → Jul 2029 expected circadian rhythm sleep disorder, delayed sleep phase type Northwestern University Recruiting No outcome recorded
NCT06412315 Feb 2025 → Oct 2026 expected depressive disorder University of Oxford Recruiting No outcome recorded
NCT05627154 May 2021 → Nov 2023 anxiety, depressive disorder University of Oxford Completed No outcome recorded
NCT05346445 Jan → Nov 2021 Hospital Regional 1o de Octubre Completed No outcome recorded
NCT04590612 Jan 2021 → Jan 2022 Parkinson disease, depressive disorder Western University, Canada Unknown No outcome recorded
NCT04169230 Oct 2019 → Sep 2020 depressive disorder University of Oxford Unknown No outcome recorded
NCT04161209 Oct 2019 → Sep 2020 depressive disorder University of Oxford Unknown No outcome recorded
NCT06212284 Feb → Nov 2018 University of Sussex Completed No outcome recorded
NCT04776226 Feb 2017 → Mar 2018 depressive disorder, stroke disorder Ege University Completed No outcome recorded
NCT04145076 Dec 2014 → Feb 2023 autism spectrum disorder King's College London Unknown No outcome recorded
Also used as a comparator or background therapy in 95 trials
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 04 trials
Phase 0 NCT03607331 Comparator Sep 2018 → Jul 2019 depressive disorder China Academy of Chinese Medical Sciences Unknown No outcome recorded
Phase 0 NCT03282110 Comparator Nov 2017 → Jun 2018 neurotic depression China Academy of Chinese Medical Sciences Unknown No outcome recorded
Phase 0 NCT04846829 Comparator Apr 2017 → Apr 2028 expected major depressive disorder University of California, Los Angeles Active not recruiting No outcome recorded
Phase 0 NCT01725048 Comparator Jan 2011 → May 2012 major depressive disorder, neoplasm UNC Lineberger Comprehensive Cancer Center Completed No outcome recorded
Phase 17 trials
Phase 1 NCT06192589 Comparator Feb → Sep 2024 drug-induced liver injury Food and Drug Administration (FDA) Completed No outcome recorded
Phase 1 NCT03516604 Comparator May 2018 → Jul 2022 depressive disorder University of Oxford Completed No outcome recorded
Phase 1 NCT01657760 Comparator May 2014 → Aug 2017 alcohol dependence VA Office of Research and Development Completed No outcome recorded
Phase 1 NCT01396720 Comparator Sep 2011 → Dec 2012 Hadassah Medical Organization Completed No outcome recorded
Phase 1 NCT01367756 Background May → Sep 2011 Hoffmann-La Roche Completed No outcome recorded
Phase 1/22 trials
Phase 1/2 NCT05271084 Background Nov 2021 → Feb 2022 major depressive disorder Hawler Medical University Completed No outcome recorded
Phase 1/2 NCT00612807 Background Jul 2006 → Jun 2010 major depressive disorder Duke University Completed No outcome recorded
Phase 213 trials
Phase 2 NCT03321526 Background Dec 2017 → Jun 2019 major depressive disorder Janssen Research & Development, LLC Completed No outcome recorded
Phase 2 NCT01937182 Comparator Sep 2013 → Dec 2016 ischemic stroke University of Aarhus Completed No outcome recorded
Phase 2 NCT01742832 Comparator May 2013 → Mar 2016 major depressive disorder University of Chicago Completed No outcome recorded
Phase 2 NCT01254305 Comparator Apr 2011 → Jul 2012 major depressive disorder Forest Laboratories Completed No outcome recorded
Phase 2 NCT01535573 Comparator Dec 2010 → Jul 2016 cocaine dependence Joy Schmitz Completed No outcome recorded
Phase 2/33 trials
Phase 2/3 NCT04777838 Comparator Mar → May 2021 myofascial pain syndrome, temporomandibular joint disorder University of Coimbra Unknown No outcome recorded
Phase 2/3 NCT01109030 Comparator Apr 2010 → Oct 2011 major depressive disorder Tehran University of Medical Sciences Completed No outcome recorded
Phase 2/3 NCT00562861 Comparator Nov 2007 → Jul 2014 bipolar depression Tufts Medical Center Completed No outcome recorded
Phase 314 trials
Phase 3 NCT06025474 Comparator Jan → Oct 2023 burning mouth syndrome Federico II University Unknown No outcome recorded
Phase 3 NCT04476030 Background Nov 2020 → Oct 2021 major depressive disorder Biogen Completed No outcome recorded
Phase 3 NCT03538691 Background Jul 2018 → Jul 2022 major depressive disorder Otsuka Pharmaceutical Development & Commercialization, Inc. Completed No outcome recorded
Phase 3 NCT02624102 Background Sep 2015 → Dec 2017 major depressive disorder Hemanny, Curt, M.D. Completed No outcome recorded
Phase 3 NCT02400346 Background Mar 2015 → Jun 2016 major depressive disorder H. Lundbeck A/S Completed No outcome recorded
Phase 431 trials
Phase 4 NCT07047651 Background Jun 2025 → Dec 2027 expected treatment-refractory schizophrenia Dr. Stavroula Rakitzi Active not recruiting No outcome recorded
Phase 4 NCT06740188 Comparator Jan 2025 → Dec 2026 expected Tongji University Recruiting No outcome recorded
Phase 4 NCT07113145 Comparator Jun 2024 → Jan 2025 premature ejaculation Beni-Suef University Completed No outcome recorded
Phase 4 NCT05735756 Comparator Jan → Apr 2022 Academic Medical Center - University of Amsterdam Terminated No outcome recorded
Phase 4 NCT05148169 Background Jan 2020 → Dec 2022 major depressive disorder Shanghai Mental Health Center Unknown No outcome recorded
Phase not applicable21 trials
NCT05957094 Comparator Aug 2023 → Aug 2024 depressive disorder, metabolic disease involving other neurotransmitter deficiency University of British Columbia Unknown No outcome recorded
NCT06358014 Background May 2023 → Dec 2024 depressive disorder Xiao Wang Unknown No outcome recorded
NCT05832619 Background Nov 2022 → Dec 2025 major depressive disorder Xiaomei Shao Unknown No outcome recorded
NCT05720637 Background Nov 2022 → Jan 2024 major depressive disorder Xiaomei Shao Completed No outcome recorded
NCT05528224 Background Sep 2022 → Aug 2023 obsessive-compulsive disorder Shanghai Mental Health Center Terminated No outcome recorded

Evidence & citations 16 cited values

Every value below carries the sentence it was read from. 198 sources stand behind the page.

FieldValueCited text
Known as Citalopram “we have restricted the IMPACT list of antidepressants to SSRIs (sertraline, escitalopram, paroxetine, fluoxetine, citalopram), duloxetine, bupropion, and mirtazapine. These...” NCT02458690
190

“Participants receive only clinical routine antidepressant treatment,Which include fluoxetine (Prozac); sertraline (Zoloft); paroxetine (Paxil); citalopram (Celexa)...” NCT01831440

“Antidepressant medications may include the following: citalopram (Celexa), escitalopram (Lexapro), paroxetine (Paxil CR), sertraline (Zoloft), venlafaxine XR (Effexor XR),...” NCT00564278

“Medication group is a control group that can choose to use the serotonin reuptake inhibitors (SSRIs) approved by China food and Drug Administration (SFDA) for the treatment of...” NCT03558256

“ADT such as citalopram, escitalopram, fluoxetine, sertraline, paroxetine, vilazodone, venlafaxine, desvenlafaxine, duloxetine or bupropion prescribed in accordance with its...” NCT01838876

Citalopram, ecitalopram, fluoxetine, sertraline, paroxetine IR, paroxetine CR, venlafaxine IR, venlafaxine XR (extended release), desvenlafaxine, duloxetine, mirtazapine,...” NCT02400346

“Drug: Antidepressant (citalopram, duloxetine, escitalopram, sertraline, or venlafaxine XR) + cariprazine (0.1-0.3 mg/d) Oral, once daily for 8 weeks following an 8 week...” NCT00854100

“The dose is 20-60mg/day for fluoxetine, 20-40mg/day for paroxetine, 100-300mg/day for fluvoxamine, 50-200mg/day for sertraline, 20-40mg/day for citalopram, 10-20mg/day for...” NCT05148169

“Participants will receive SSRI antidepressant (such as, citalopram, escitalopram, fluvoxamine, fluoxetine, paroxetine, sertraline, vilazodone or vortioxetine) as a part of...” NCT03321526

“Antidepressant medications may include any of the following: citalopram, escitalopram, paroxetine, sertraline, venlafaxine XR, bupropion SR, duloxetine, nortriptyline, and mirtazapine.” NCT00742573

“approved by the State Food and Drug Administration (CFDA) for the treatment of OCD (i.e., fluoxetine, paroxetine, sertraline and fluvoxamine) as well as citalopram and escitalopram” NCT05528224

“SSRIs antidepressants, including fluoxetine, paroxetine, sertraline, citalopram, etc., will be administered at oral doses determined by the psychiatrist. Once daily for 6 weeks.” NCT05832619

“quantifying the range of concentration to citalopram, escitalopram, sertraline, fluoxetine, paroxetine, fluvoxamine, duloxetine and venlafaxine in mother plasma and breast milk” NCT01796132

“This study uses SSRIs class drugs, including fluoxetine, paroxetine, fluvoxamine, sertraline, citalopram, and escitalopram, with no specific restrictions on the type of drugs.” NCT06358014

“ADT such as bupropion, citalopram, desvenlafaxine, duloxetine, escitalopram, fluoxetine, sertraline, venlafaxine, paroxetine or vilazodone as prescribed by the physician.” NCT01715805

“Throughout the study, all subjects will receive either escitalopram (Lexapro) or citalopram (Celexa) on the basis of the study doctor's clinical judgment.” NCT00361218

“SSRIs antidepressants, including fluoxetine, paroxetine, sertraline, citalopram, etc., will be administered at oral doses determined by the psychiatrist.” NCT05720637

“SSRIs antidepressants, including fluoxetine, paroxetine, sertraline, citalopram, etc., will be administered at oral doses determined by the psychiatrist.” NCT05605002

“Patients who are not on a SSRI at the time of enrollment will be prescribed citalopram 10 mg per day for 2 weeks, then 20 mg per day.” NCT00129467

“Patients with MDD, in use of antidepressants (fluoxetine, citalopram, escitalopram, bupropion, etc.) without psychotherapy.” NCT02624102

“Received Citalopram hydrobromide, starting with 10 mg once daily for 1 week, followed by 20 mg once daily for 10 weeks” NCT07113145

“SSRIs (daily dose of at least 20 mg for citalopram, 20 mg for fluoxetine, 100 mg for sertraline, 20 mg for paroxetine)” NCT00612807

“selective serotonin reuptake inhibitors (fluoxetine, sertraline, citalopram, escitalopram, paroxetine or fluvoxamine)” NCT03993535

“sertraline: 100-200mg, citalopram 20-40mg, escitalopram 10-20mg, paroxetine 20-60mg; fluoxetine 20-80mg” NCT01903447

“Patients will receive the "treatment as usual" with a SSRI: sertraline or citalopram.” NCT02262156

“selective serotonin reuptake inhibitor (SSRI; paroxetine or citalopram; n = 34)” PMID 26663632 Dec 2015

“Fluoxetine, escitalopram, citalopram, fluvoxamine, or sertraline” NCT03222570

“paroxetine, fluoxetine, sertraline, escitalopram, citalopram” NCT00944996

“either citalopram 20 mg/day or fluvoxamine 100 mg/day” PMID 25689244 Feb 2015

citalopram (20 mg, increased to 30 to 40 mg)” NCT00118430

“paroxetine (Paxil); citalopram (Celexa)” NCT01460212

“escitalopram, citalopram or sertraline” NCT02279953

“- Citalopram 20-60 mg/d. N06AB04” NCT01305707

citalopram (Celexa and others)” NCT01944657

Citalopram (Celexa)10-60;” NCT00074815

citalopram 20-60mg/day” NCT02023567

Citalopram, Celexa” NCT01916824

citalopram_Celexa” NCT00817011

CitalopramNCT00864890

CitalopramNCT00865085

citalopramNCT00157547

NCT02374567

NCT00562861

NCT02237937

NCT00188396

NCT01473381

NCT00876226

NCT00271596

NCT04161209

NCT03779789

NCT06740188

NCT03278938

NCT02285699

NCT00048815

NCT00993876

NCT06796946

NCT00666757

NCT00609531

NCT01778686

NCT01153165

NCT00221494

NCT00108563

NCT00613470

NCT01575158

NCT01424384

NCT06412315

NCT00962039

NCT00977353

NCT00376051

NCT05588102

NCT00774813

NCT00939835

NCT00433121

NCT00676039

NCT03907215

NCT00893256

NCT00940238

NCT00208572

NCT01032083

NCT02022709

NCT00594269

NCT04846829

NCT01300364

NCT05271084

NCT01109030

NCT00538889

NCT01179568

NCT05957094

NCT02113943

NCT02000726

NCT06212284

NCT00226694

NCT01657760

NCT00351910

NCT00073658

NCT02825342

NCT01154647

NCT01099592

NCT01951053

NCT00865943

NCT04766229

NCT01716221

NCT00021528

NCT00254020

NCT00254007

NCT00692445

NCT05346445

NCT00477165

NCT04777838

NCT00680602

NCT01658228

NCT00602290

NCT00672659

NCT04497168

NCT00047671

NCT05063604

NCT03282110

NCT03499171

NCT02655354

NCT00162916

NCT02711215

NCT00297505

NCT00018902

NCT00317746

NCT01535573

NCT00794040

NCT00047450

NCT00067301

NCT06017037

NCT01436643

NCT00898807

NCT01254305

NCT02179268

NCT03607331

NCT04355455

NCT03746691

NCT01189812

NCT01978782

NCT01312922

NCT00249405

NCT03899285

NCT05735756

NCT02092974

NCT01032018

NCT01725048

NCT01557946

NCT04776226

NCT00834834

NCT00532519

NCT04169230

NCT00955474

NCT04590612

NCT00864890

NCT06025474

NCT00249886

NCT01667744

NCT02028026

NCT01041274

NCT06949644

NCT00896441

NCT00080158

NCT05041582

NCT04975724

NCT04097288

NCT01367756

NCT00269334

NCT04476030

NCT06192589

NCT01946607

NCT02080832

NCT00009204

NCT00865085

NCT00825825

NCT00217828

NCT01742832

NCT04145076

NCT01216449

NCT03516604

NCT00218036

NCT00838305

NCT01764867

NCT01937182

NCT02473250

NCT03854578

NCT00015548

NCT00044798

NCT01896349

NCT05627154

NCT01919216

NCT02386475

NCT02269540

Known as Celexa “Participants receive only clinical routine antidepressant treatment,Which include fluoxetine (Prozac); sertraline (Zoloft); paroxetine (Paxil); citalopram (Celexa)...” NCT01831440
16

“Antidepressant medications may include the following: citalopram (Celexa), escitalopram (Lexapro), paroxetine (Paxil CR), sertraline (Zoloft), venlafaxine XR (Effexor XR),...” NCT00564278

“This study will evaluate the effectiveness of the stimulant medication methylphenidate (MPH, more commonly known as Ritalin ) when combined (or not combined) with the...” NCT00794040

“Throughout the study, all subjects will receive either escitalopram (Lexapro) or citalopram (Celexa) on the basis of the study doctor's clinical judgment.” NCT00361218

“METHOD: Effexor XR/Novo-venlafaxine XR 75 mg and Celexa/Gen-citalopram 40 mg were studied in a randomized crossover design.” PMID 19653973 Jul 2009

“This study will compare the safety and effectiveness two medications, citalopram (Celexa®) and risperidone (Risperdal®).” NCT00073658

“We will administer MDMA alone and in combination with the antidepressant citalopram (one trade name for this is Celexa).” NCT00838305

“antidepressant therapy with Celexa (Citalopram) in people suffering from Major Depressive Disorder.” NCT00067301

“Participants receive citalopram (Celexa) for 8 weeks and a placebo for 1 week.” NCT00047671

“Participants will take citalopram (Celexa)” NCT00047450

“citalopram hydrobromide (Celexa®) tablets” NCT03538691

“citalopram (Celexa and others)” NCT01944657

“Citalopram (Celexa)10-60;” NCT00074815

“Citalopram [Celexa]” NCT00009204

“citalopram (celexa)” NCT00254007

“citalopram_CelexaNCT00817011

NCT02178696

Known as CelexaTM CelexaTM 40 mg tablets, single dose” NCT00865085
Known as cipralex “citalopram (cipralex)” NCT00532519
Known as Cipramil “50 patients with reflux hypersensitivity and 50 patients with functional heartburn will receive either placebo or citalopram (Cipramil®) 20 mg as an add-on for a period of 8 weeks.” NCT03499171
Known as CIT “OBJECTIVE: To confirm the efficacy of a targeted complicated grief treatment (CGT), determine whether citalopram (CIT) enhances CGT outcome, and examine CIT efficacy without CGT.” PMID 27276373 Jul 2016
1

“Pipamperone/Citalopram (PNB01) Versus Citalopram (CIT) and Versus Pipamperone (PIP) in Major Depressive Disorder (MDD)” NCT01312922

Known as Citalopram Aurobindo “The medicinal product Citalopram Aurobindo contains citalopram as active ingredient available on the market in 20 mg film coated tablets. The tablets are divisible in two equal...” NCT04975724
Known as Citalopram HBr Citalopram HBr eq. 10 mg tablets, single dose” NCT00865943
2

Citalopram HBr 40 mg tablets, single dose” NCT00865085

Citalopram HBr 40 mg tablets, single dose” NCT00864890

Known as Citalopram hydrobromide Citalopram Hydrobromide Tablets 40 mg: Test Product: Citalopram Hydrobromide Tablets 40 mg manufactured by Torrent Pharmaceuticals Limited, India” NCT00940238
5

“the control group was given citalopram hydrobromide combined with zolpidem” NCT06740188

citalopram hydrobromide (Celexa®) tablets” NCT03538691

NCT00086645

NCT00930293

NCT00363909

Known as Citalopram, Celexa “citalopram (Celexa)” NCT01460212
1

Citalopram, CelexaNCT01916824

Known as CTP “OBJECTIVE: Despite the clinical importance of chronic and severe irritability, there is a paucity of controlled trials for its pharmacological treatment. Here, we examine the...” PMID 31128268 May 2019
Known as Gen-Citalopram “METHOD: Effexor XR/Novo-venlafaxine XR 75 mg and Celexa/Gen-citalopram 40 mg were studied in a randomized crossover design.” PMID 19653973 Jul 2009
Known as seropram ClinicalTrials.gov intervention name — accepted as the source's own label NCT07047651
Action Inhibit “citalopram, a selective serotonin reuptake inhibitor (SSRI)” NCT00217828
Modality Small molecule “citalopram, another SSRI” NCT00834834
Route Oral “taken orally” NCT00048815