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NCT07787689Possibly a fitNot yet recruiting

Steroid schedules for boys with Duchenne muscular dystrophy

Duchenne Muscular Dystrophy

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

This study compares two ways of taking the steroid prednisolone (every day vs. every other day) to see which works better for boys with Duchenne muscular dystrophy who can still walk. It aims to find a schedule that helps manage symptoms with fewer side effects.

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

Phase
N/A
Enrollment
40 people
Ages
4 years to 10 years
Study type
Interventional

Who can take part

  • Male, aged 4 to 10 years
  • Diagnosis of Duchenne muscular dystrophy confirmed by genetic testing
  • Elevated creatine kinase (CK) levels (over 1000 U/L) with typical symptoms
  • Able to walk and complete basic mobility tests
  • No serious heart or lung problems

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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