drugset / Trial / NCT00000492

Beta-Blocker Heart Attack Trial (BHAT)

NCT00000492

RandomizedDouble-blindPrevention

Summary

To determine whether the regular administration of the beta-blocker drug propranolol to people who had had at least one documented myocardial infarction would result in a significant reduction of mortality from all causes over the follow-up period. Eligible volunteer patients were recruited to participate in a double-blind clinical trial within 21 days after the onset of the acute event. One-half of the patients were randomly assigned to a beta-blocking drug (propranolol) and one-half to a placebo. The trial also evaluated the effect of propranolol on incidences of coronary heart disease mortality, sudden cardiac death, and nonfatal myocardial infarction plus coronary heart disease mortality in persons with documented previous myocardial infarction.

Timeline

Start
1977-09
Primary completion
Completion
1981-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Propranolol Small molecule 240 mg