drugset / Trial / NCT00624065

Research Study To Test Carvedilol CR + Lisinopril Versus Lisinopril + Placebo In Patients With High Blood Pressure

NCT00624065

Phase 3 Completed 348 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindTreatment

Summary

Randomized, double-blind, parallel group, multicenter study of subjects with Stage 1 or 2 essential hypertension who are not at target blood pressure (\<140/90mmHg) at Baseline. Subjects will be randomized to receive either carvedilol CR + lisinopril or lisinopril + placebo. Subjects will be uptitrated over a 6 week period until target blood pressure (\<140/90mmHg) is met. The primary objective of the study is to compare the proportion of subjects who achieve target blood pressure after 6 weeks of treatment.

Timeline

Start
2008-03
Primary completion
2008-08
Completion
2008-08

Publications

  • Background GSK has submitted manuscripts of these study results to peer-reviewed scientific journals which were not accepted for publication. GSK is providing the attached study results summary with a conclusion.

Drugs

EvaluationDrugModalityDoseRoute
Subject Carvedilol Other / unclassified
Subject LISINOPRIL ANHYDROUS Small molecule