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Beta-blocker Discontinuation in Heart Failure With Preserved Ejection Fraction
Recruiting
Effect of Beta-blocker Discontinuation on Functional Capacity and Cardiac Hemodynamics in Patients With Heart Failure With Preserved Ejection Fraction
Who can join
Ages 50 to 80 · All sexes
Full eligibility criteria
Inclusion Criteria: * Stable HFpEF patients with NYHA Class II-III or elevated BNP ≥100 * N=30 (Target: 30). * Age: 50 \~ 80 years. * ECHO evidence of EF ≥50% and Grade 2 or 3 diastolic dysfunction. * Chronic loop diuretic use * Currently on beta-blocker Exclusion Criteria: * Beta blocker was prescribed for treating other cardiac conditions such as atrial fibrillation or coronary artery disease. * Heart rate \> 100 bpm * Recent hospitalization due to HF within 3 months * Non-English speaker
About the study
This is a prospective pilot study to evaluate changes before and 4 weeks after beta-blocker withdrawal in 30 HFpEF patients.
What is being tested
- beta blocker discontinuation (other)
Sponsor: UConn Health · Participants: 30 · Started: Dec 20, 2021
Contact the study team
- Kai Chen, MD,PhD · Phone: 860-679-3343
Official record on ClinicalTrials.gov — NCT05174351
Locations in the U.S.
| Connecticut | UConn Health / John Dempsey Hospital, Farmington |
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.