Clin2
NCT07402122Likely a fitNot yet recruiting

Registry for Duchenne and Becker muscular dystrophy

Duchenne Muscular Dystrophy (DMD)Becker Muscular DystrophyDystrophinopathy Symptomatic Female Carrier

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

This study collects information from patients with Duchenne or Becker muscular dystrophy to learn more about the conditions and improve care. You will share data through a telemedicine platform, and you need a smartphone or tablet to take part.

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

Phase
N/A
Enrollment
1,500 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a confirmed genetic diagnosis of Duchenne or Becker muscular dystrophy
  • If you are a female carrier, you must have symptoms of the condition
  • You are being treated at one of the participating centers
  • You can understand the study and sign a consent form (or a parent can do it for you)
  • You have a smartphone or tablet to use the telemedicine platform
  • You agree to share your data with your doctors and the registry

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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