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RecruitingNCT05174351HFpEF-BBUpdated Sep 29, 2025

Beta-blocker Discontinuation in Heart Failure With Preserved Ejection Fraction

An interventional study of beta blocker discontinuation in Heart Failure With Preserved Ejection Fraction, sponsored by UConn Health. Recruiting at 1 site in United States. Open to participants aged 50 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-09-29.

Sponsored by UConn Health · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Dec 2021; still recruiting 4 years 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
50 Years to 80 Years
Sex
All
01

Study summary

This is a prospective pilot study to evaluate changes before and 4 weeks after beta-blocker withdrawal in 30 HFpEF patients.

Read the detailed description

This is a prospective pilot study to evaluate changes before and 4 weeks(+/- 1 week) after beta-blocker withdrawal in 30 HFpEF patients. The study involves 2 visits that are 4 weeks apart. The first study visit will occur at a standard of care clinic visit and the second visit will be a research visit to fill out questionnaires and perform the limited echocardiogram. No long term follow up beyond the 2nd visit.

02

Conditions studied

  • Heart Failure With Preserved Ejection Fraction

Keywords

  • HFpEF
  • Beta-blocker
  • echocardiogram
  • 6MWT
03

In context

Lead sponsor

UConn Health is the lead sponsor of 182 studies on the registry; 18 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 6 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    HFpEF patients

    HFpEF patient who are currently taking beta blockers

    Other: beta blocker discontinuation

Interventions

  • Otherbeta blocker discontinuation

    beta blocker discontinuation

06

What researchers measure

Primary outcomes

  1. Changes in KCCQ-23 score

    Kansa city cardiomyopathy questionnaire (KCCQ-23)- self-administered, 23-item. questionnaire that quantifies physical limitations, symptoms, self-efficacy, social interference and quality of life. Scores are transformed to a range of 0-100, where higher scores reflect better health status.

    Time frame: Baseline and after 4 weeks of beta blocker discontinuation

Secondary outcomes

  1. Changes in cardiac mechanics by echocardiography

    Echocardiographic E/e' ratio

    Time frame: Baseline and after 4 weeks of beta blocker discontinuation

  2. Changes in biomarker

    changes from baseline in BNP level (pg/mL) after 4 weeks of beta blocker discontinuation

    Time frame: Baseline and after 4 weeks of beta blocker discontinuation

  3. 6 minute walk test

    The distance (meters) covered over a time of 6 minutes. A greater distance indicates a better exercise capacity.

    Time frame: Baseline and after 4 weeks of beta blocker discontinuation

07

Study locations

1 of 1 sites recruiting
  • UConn Health / John Dempsey Hospital
    Farmington, Connecticut 06030, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 29, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05174351
Lead sponsor
UConn Health
Responsible party
Christopher Pickett (Associate Professor, UConn Health) — Principal investigator
First posted
Dec 30, 2021
Start date
Dec 20, 2021
Primary completion
Nov 1, 2027 (estimated)
Completion
Nov 1, 2027 (estimated)
Last update
Sep 29, 2025

Study contacts

Kai Chen, MD,PhD
Contact
kachen@uchc.edu
860-679-3343
Kai Chen, MD,PhD
principal investigator · UConn Health

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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