Clin2
NCT06917430Possibly a fitNot yet recruiting

AI muscle scans for inherited muscle diseases

Becker Muscular DystrophyFSHD - Facioscapulohumeral Muscular DystrophyHypokalemic Periodic Paralysis

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

This study uses MRI scans and artificial intelligence to better understand muscle changes in people with inherited muscle diseases. The results may help doctors plan treatments and monitor these conditions more accurately.

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

Phase
N/A
Enrollment
120 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years or older.
  • You have a genetically confirmed diagnosis of a neuromuscular disease (like muscular dystrophy or other inherited muscle conditions).
  • You are able to have an MRI scan (no metal implants, pacemaker, or severe claustrophobia).
  • You do not have other muscle disorders that could interfere with the measurements.

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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