drugset / Trial / NCT00882440

A Study to Investigate the Efficacy and Safety of Different Doses of Losartan Potassium (MK0954-011)

NCT00882440

Phase 3 Completed 576 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study was to compare the antihypertensive efficacy of different doses of losartan compared to placebo and enalapril, in patients with supine diastolic blood pressure of 100-115 mmHg.

Timeline

Start
1990-12
Primary completion
1991-08
Completion
1992-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Enalapril Other / unclassified 20 mg Oral
Subject Losartan Other / unclassified 10 mg Oral
Subject Losartan Other / unclassified 25 mg Oral
Subject Losartan Other / unclassified 50 mg Oral
Subject Losartan Other / unclassified 100 mg Oral
Subject Losartan Other / unclassified 150 mg Oral

Indications