Rare muscle disease study seeks clues in one Patient's tissue
NCT ID NCT06096441
First seen Nov 01, 2025 · Last updated May 12, 2026 · Updated 27 times
Summary
This study aimed to learn more about facioscapulohumeral muscular dystrophy (FSHD) by examining muscle tissue from people with the condition. Researchers planned to look for biological markers that could help understand the disease better. Only one person took part before the study was stopped.
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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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Contacts and locations
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Locations
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The Abigail Wexner Research Institute at Nationwide Children's Hospital
Columbus, Ohio, 43205, United States
Conditions
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