Status:

COMPLETED

Beta-Blocker Evaluation in Survival Trial (BEST)

Lead Sponsor:

National Heart, Lung, and Blood Institute (NHLBI)

Conditions:

Cardiovascular Diseases

Heart Diseases

Eligibility:

All Genders

18-100 years

Phase:

PHASE3

Brief Summary

To determine if addition of a beta-blocker to standard therapy in Class III and Class IV heart failure patients reduced total mortality.

Detailed Description

BACKGROUND: Controlled and uncontrolled studies suggested that beta-blockade improves ventricular function in congestive heart failure. Several trials suggested that beta-blockers may also reduce mor...

Eligibility Criteria

Men and women, ages 18 and over. Patients had compensated congestive heart failure due to idiopathic dilated cardiomyopathy or coronary disease with ejection fraction less than or equal to 0.35, were in the New York Heart Association functional class III or IV, and were taking an angiotensin-converting enzyme inhibitor, digitalis, and if needed, a diuretic. Patients with a specific indication for, or contraindication to, beta-blockade were excluded.

Key Trial Info

Start Date :

June 1 1994

Trial Type :

INTERVENTIONAL

End Date :

September 1 1999

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT00000560

Start Date

June 1 1994

End Date

September 1 1999

Last Update

April 14 2016

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Beta-Blocker Evaluation in Survival Trial (BEST) | DecenTrialz