Clin2
NCT06290713Likely a fitRecruiting

Blood flow and exercise study for Duchenne muscular dystrophy

Duchenne Muscular DystrophyDuchenne DiseaseMuscular DystrophyMuscular Dystrophy in ChildrenVasodilationExerciseDMD

Treatments studied

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

This trial tests if a medicine that improves blood flow, combined with exercise, can help muscles in boys with Duchenne muscular dystrophy. It is for boys who can still walk and are on a stable steroid medication.

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

Phase
Phase 2
Enrollment
50 people
Ages
6 years and older
Study type
Interventional

Who can take part

  • You have a genetic diagnosis of Duchenne muscular dystrophy.
  • You are at least 6 years old.
  • You can still walk without help.
  • You are on a stable dose of steroid medicine for at least 3 months.
  • You do not have any medical conditions that would make MRI unsafe or affect muscle function.
  • You are not taking certain heart medicines or other investigational drugs.

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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