This study is a contribution of Temple Cardiology to a multi-institutional trial supported by NIH. The hypothesis tested is that amiodarone or an implantable cardioventer-defibrillator (ICD) will improve survival compared to placebo in patients with an LVEF less than, or equal to 35% and NYHA class II or III heart failure without VT or VF. Fifty patients will be accrued at Temple over 2.5 years with 2.5 year follow up in 50 institutions. The drug and placebo aims are blinded but not, of course, the ICD. The primary criterion is mortality.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000349-34
Application #
6420646
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2000-12-01
Project End
2001-11-30
Budget Start
Budget End
Support Year
34
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Temple University
Department
Type
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19122
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