drugset / Trial / NCT00269243

Management With Accupril Post Bypass Graft

NCT00269243

RandomizedParallel-groupDouble-blind

Summary

Angiotensin converting enzyme (ACE) inhibitors have been shown to improve survival and to reduce the risk of cardiovascular events in some groups of patients following myocardial infarction. This study is designed to test whether early initiation (≤7 days) of an ACE inhibitor post-coronary artery bypass graft (CABG), would reduce cardiovascular events. The trial was a double-blind, placebo controlled study of 2,553 patients randomly assigned to quinapril, target dose 40 mg daily or placebo, followed up to 43 months.

Timeline

Start
1999-11
Primary completion
Completion
2005-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Quinapril Small molecule 40 mg

Indications

No indication recorded.