drugset / Trial / NCT01204398

Telmisartan+Amlodipine Fixed Dose Combination in Hypertension

NCT01204398

Phase 3 Completed 27 enrolled Boehringer Ingelheim
RandomizedSingle-groupOpen-labelTreatment

Summary

The primary objectives of this trial is to evaluate the changes from baseline (Visit 2) in the 24-hour Ambulatory Blood Pressure Monitoring mean (relative to dose time) for diastolic blood pressure and systolic blood pressure after 8 weeks of treatment with Telmisartan 80mg/Amlodipine 5mg in patients with moderate to severe hypertension

Timeline

Start
2010-11
Primary completion
2011-07
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Amlodipine Other / unclassified 5 mg
Subject Telmisartan Other / unclassified 80 mg

Indications