drugset / Trial / NCT02242318

Study to Evaluate Efficacy of Micardis® (Telmisartan) and Valsartan in Patients With Mild-to-moderate Hypertension After Missing One Dose Using Ambulatory Blood Pressure Monitoring

NCT02242318

Phase 4 Completed 440 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary aim of the trial is to compare telmisartan 80 mg to valsartan 160 mg in lowering diastolic blood pressure in patients who missed a dose of their medication, as measured by ABPM (change from baseline in mean DBP over 24 hours), and to compare telmisartan 80 mg to valsartan 160 mg in lowering DBP during the last six hours of the dosing interval at the end of a 6 to 8-week treatment period, as measured by ABPM (change from baseline)

Timeline

Start
2001-09
Primary completion
2002-09
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Telmisartan Other / unclassified 80 mg Oral
Comparator Valsartan Small molecule 160 mg Oral

Indications