drugset / Trial / NCT00383929

Antihypertensive Efficacy and Safety of Candesartan/HCT 32/12.5 and 32/25 mg in Comparison With Candesartan 32 mg

NCT00383929

Phase 3 Completed 1979 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

In this study it is intended to compare the blood pressure lowering effect of the combination of candesartan cilexetil (candesartan) 32 mg and hydrochlorothiazide (HCT) 25 mg and the combination of candesartan 32 mg and HCT 12.5 mg to that of candesartan 32 mg alone in patients whose blood pressure is not well controlled on candesartan 32 mg monotherapy. The Primary Objectives are to compare sitting BP lowering effect of candesartan/HCT 32/25 mg and candesartan/HCT 32/12.5 mg with that of candesartan 32 mg, respectively.

Timeline

Start
2006-09
Primary completion
2007-08
Completion
2007-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Candesartan cilexetil Unknown 32 mg Oral
Subject Hydrochlorothiazide Unknown 12.5 mg Oral
Subject Hydrochlorothiazide Unknown 25 mg Oral

Indications