Exercise test could be key to tracking rare muscle disease treatment
NCT ID NCT03802279
First seen Nov 01, 2025 · Last updated Apr 28, 2026 · Updated 26 times
Summary
This study looked at whether an exercise test can be used to monitor treatment in people with a rare inherited disease that causes sudden muscle breakdown (rhabdomyolysis). Researchers measured heart function and oxygen use during exercise in 27 patients. The goal was to find better ways to track disease severity and response to new therapies in future clinical trials.
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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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Hôpital Necker-Enfants Malades
Paris, 75015, France
Conditions
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