500-Patient study aims to speed up diagnosis of rare nerve and muscle diseases
NCT ID NCT04417023
First seen Jan 07, 2026 · Last updated May 21, 2026 · Updated 24 times
Summary
This study enrolls 500 adults with neuromuscular diseases to collect blood, tissue, and imaging data. The goal is to identify genetic markers and other clues that can help doctors diagnose these rare conditions faster and better understand how the diseases progress. Participants provide samples during routine care, and the findings may lead to future treatments.
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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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Ottawa Hospital Research Institute
Ottawa, Ontario, K1Y4E9, Canada
Conditions
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