This study will primarily assess the safety of Carvedilol and secondarily the effect of symptoms on NYHA Class at the maximally allowed dose during twelve months of twice daily dosing in patients who have completed a double-blind protocol with Carvedilol and have symptome of NYH Class I-IV Congestive Heart Failure.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000645-28S1
Application #
6220010
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
28
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
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