Myocarditis Treatment Trial

Sponsor
University of Utah (Other)
Overall Status
Completed
CT.gov ID
NCT00000524
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
92

Study Details

Study Description

Brief Summary

To determine whether immunosuppressive treatment improved cardiac function in patients with biopsy-proven myocarditis.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

BACKGROUND:

Heart failure due to myocarditis can be a devastating illness. At the same time, immunosuppressive therapy is associated with considerable risks of untoward side effects. Clinicians did not know whether, under what circumstances, or in what form, this hazardous treatment should be used in such critically ill patients. In addition, if immunosuppressive therapy was of benefit, then endomyocardial biopsy in patients suspected of having myocarditis was a justified procedure. The trial also provided information concerning the side effects of immuno-suppressive therapy in such patients.

DESIGN NARRATIVE:

Patients were randomized into two treatment arms consisting of conventional therapy alone for congestive heart failure or combined with a twenty-four week regimen of immunosuppressive therapy. Immunosuppressive therapy consisted of prednisone with either cyclosporine or azathioprine. The primary outcome measure was a change in the left ventricular ejection fraction at twenty-eight weeks. Secondary endpoints included survival, failures of therapy, requirements for conventional therapy, assessments of symptoms, myocardial histology, and arrhythmias.

The study completion date listed in this record was obtained from the Query/View/Report (QVR) System.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Primary Purpose:
Treatment
Study Start Date :
Jul 1, 1986
Actual Study Completion Date :
Mar 1, 1994

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Men and women, 18 years of age or older, with left ventricular failure and biopsy-documented myocarditis.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Utah
    • National Heart, Lung, and Blood Institute (NHLBI)

    Investigators

    • : Jay Mason, University of Utah

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00000524
    Other Study ID Numbers:
    • 43
    • R01HL034744-04
    First Posted:
    Oct 28, 1999
    Last Update Posted:
    Nov 27, 2013
    Last Verified:
    Nov 1, 2013

    Study Results

    No Results Posted as of Nov 27, 2013