Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
All Genders
NCT07054489

UPBEAT: Using Polygenic Scores to Guide BB Therapy in HF With Mildly Reduced EF

Led by David Lanfear · Updated on 2026-05-07

10

Participants Needed

1

Research Sites

61 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will use polygenic scores, a tool which describes differences in genetics, to examine effectiveness of beta blocker medication in heart failure patients with ejection fraction of 41-50 percent. The study will also assess beta blockers' effect on the changes in left ventricular end-systolic volume index by MRI.

CONDITIONS

Official Title

UPBEAT: Using Polygenic Scores to Guide BB Therapy in HF With Mildly Reduced EF

Who Can Participate

Age: 18Years - 89Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-89 years
  • Ejection Fraction (EF) >40% and <=50% by any test within 1 year (most recent required)
  • Clinical diagnosis of heart failure within 1 year, shown by hospital discharge with HF diagnosis, emergency room discharge for HF, outpatient HF diagnosis with diuretic use, or elevated BNP/NTproBNP levels
  • Ability to fully participate in study activities without long travel limitations
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Previous ejection fraction <=35%
  • Currently taking beta blockers at or above 25% of the target dose
  • Uncontrolled high blood pressure (systolic >180 at enrollment)
  • Contraindications to all beta blockers or intolerance to metoprolol
  • Low blood pressure (systolic <100) or heart rate <70
  • Active cancer treatment
  • History of heart transplant or left ventricular assist device or expected within one year
  • Life expectancy less than 1 year
  • Dialysis dependence or end-stage renal disease
  • Recent (within 90 days) or planned heart attack, PCI, or cardiac surgery
  • Absolute need for beta blockers for other reasons besides heart failure
  • Contraindication to MRI procedures
  • Investigator decision that participation is not in patient's best interest

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Henry Ford Health

Detroit, Michigan, United States, 48202

Actively Recruiting

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Research Team

W

Whitney Cabral, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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