Coronary Drug Project Mortality Surveillance

NCT00000483 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL

Last updated 2013-11-26

No results posted yet for this study

Summary

To determine whether there were any long term sequelae of the drugs used in the Coronary Drug Project (estrogens, dextrothyroxine, nicotinic acid, clofibrate).

Conditions

Interventions

DRUG

estrogen

DRUG

clofibrate

DRUG

dextrothyroxine sodium

DRUG

niacin

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    lead NIH

Principal Investigators

  • Roger Sherwin · University of Maryland

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION

Eligibility

Min Age
30 Years
Max Age
64 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
1981-06-30
Completion
1985-03-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00000483 on ClinicalTrials.gov