2,000
Participants
Start Date
August 17, 2025
Primary Completion Date
June 1, 2031
Study Completion Date
July 1, 2031
Metoprolol Succinate
Metoprolol succinate is a beta-blocker used for the management of heart failure with reduced ejection fraction (HFrEF). In this study, participants in the metoprolol succinate group will remain on their current treatment regimen with metoprolol succinate. The dose will be titrated to the recommended target dose as per the study protocol. The intervention aims to evaluate the effectiveness of continued use of metoprolol succinate in patients with heart failure and an implantable cardioverter defibrillator (ICD).
Carvedilol
Carvedilol is a non-selective beta-blocker with alpha-blocking activity used in the treatment of heart failure. In this study, participants assigned to the carvedilol group will switch from metoprolol succinate to carvedilol at an equivalent dose. The carvedilol dose will be titrated to recommended target doses according to the study protocol. This intervention aims to compare the effectiveness of carvedilol versus metoprolol succinate in improving clinical outcomes in patients with heart failure and ICDs.
RECRUITING
Suny Downstate, Brooklyn
RECRUITING
New York-Presbyterian Brooklyn Methodist Hospital, Brooklyn
RECRUITING
University of Rochester Medical Center, Rochester
RECRUITING
Virginia Commonwealth University, Richmond
RECRUITING
AdventHealth Redmond, Rome
RECRUITING
Henry Ford Health System, Detroit
RECRUITING
University of Wisconsin Hospital and Clinics, Madison
RECRUITING
University of Mossouri, Columbia
RECRUITING
AdventHealth Shawnee Mission, Shawnee Mission
RECRUITING
Creighton University Medical Center, Omaha
RECRUITING
CHRISTUS Trinity Mother Frances Health System, Tyler
RECRUITING
Health University of Utah, Salt Lake City
RECRUITING
HonorHealth, Scottsdale
Patient-Centered Outcomes Research Institute
OTHER
University of Rochester
OTHER