drugset / Trial / NCT00550953

Filtered Trial for Telmisartan 40mg Non-responder

NCT00550953

Phase 3 Completed 314 enrolled Boehringer Ingelheim
Parallel-groupTreatment

Summary

The primary purpose of this study is to: Demonstrate that a fixed-dose combination of telmisartan 40 mg plus amlodipine 5 mg is superior to telmisartan 40 mg alone in patients with essential hypertension and inadequately controlled with telmisartan 40 mg monotherapy.

Timeline

Start
2007-10
Primary completion
2008-07
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Amlodipine Other / unclassified 5 mg
Subject Telmisartan Other / unclassified 40 mg