Researchers hunt for muscle clues in rare dystrophy
NCT ID NCT01851447
First seen Jun 27, 2026 · Last updated Jul 01, 2026 · Updated 3 times
Summary
This pilot study looks at biomarkers in the blood of people with fragile sarcolemmal muscular dystrophy, a condition that makes muscle membranes weak. Researchers will collect blood samples at rest and after exercise during four 5-day hospital stays. The goal is to better understand how the disease affects muscles, which could guide future treatments. No treatment is given in this study.
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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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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States