New study aims to uncover muscle clues in rare dystrophy
NCT ID NCT01851447
First seen Sep 30, 2025 · Last updated May 15, 2026 · Updated 29 times
Summary
This study looks at blood markers (enzymes) in adults with a type of muscular dystrophy that makes muscle membranes fragile. Researchers want to see how these markers change with rest and exercise. The goal is to better understand the disease, not to provide treatment. Participants will make four 5-day visits to the NIH for blood draws, physical tests, and imaging.
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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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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
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