Clin2
NCT05066633Possibly a fitRecruiting

Metoprolol added to standard care to prevent heart muscle damage

Muscular Dystrophy, Duchenne

Treatments studied

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This trial tests whether adding metoprolol (a beta-blocker) to usual care can prevent or slow cardiomyopathy (heart muscle weakness) in people with Duchenne muscular dystrophy (DMD). It also checks for safety, especially effects on heart rate and rhythm.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
150 people
Ages
8 years to 17 years
Study type
Interventional

Who can take part

  • A parent/legal guardian agrees in writing (and you can assent if you’re old enough) before any study steps
  • You can take pills by mouth and are willing to take the study medicine as instructed for the whole study
  • You have a confirmed diagnosis of DMD based on genetic test results or lab tests showing missing/damaged dystrophin protein
  • You have been taking an ACE inhibitor (ACEi) medication at the required dose for at least 30 days
  • You are not currently taking (and have not permanently used) any beta-blocker medication in the past
  • Your heart health looks safe for this study: no pacemaker/ICD, no heart failure symptoms, no significant slow heart rhythm or certain heart block patterns, and ejection fraction is at least 57%

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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