New study follows muscle decline in rare muscular dystrophy
NCT ID NCT06390566
First seen Jan 15, 2026 · Last updated Apr 29, 2026 · Updated 16 times
Summary
This study follows 25 people with limb-girdle muscular dystrophy 2A (LGMD2A) to measure how their muscle strength and quality of life change over time. Participants must have a confirmed genetic diagnosis and be able to perform muscle tests. The goal is to better understand the natural course of the disease, not to test a treatment.
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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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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Locations
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Hôpital Henri Mondor
Créteil, Île-de-France Region, 94130, France
Conditions
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