New study aims to map muscle disease progression in kids
NCT ID NCT07511920
First seen Apr 13, 2026 · Last updated May 08, 2026 · Updated 6 times
Summary
This study will follow 500 boys with Duchenne or Becker muscular dystrophy over time to understand how their condition changes. Researchers will measure muscle function, body composition, and lab tests to create a model that predicts disease progression. The goal is to help doctors personalize care and plan better treatments in the future.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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West China Second University Hospital, Sichuan University
Chengdu, China
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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