NIH launches major study to map rare muscle disease
NCT ID NCT06287762
Summary
This study aims to better understand RYR1-related disorders, a group of rare genetic conditions that cause muscle weakness. Researchers will track 150 children and adults with the condition over 3 to 5 years, collecting detailed health information through annual visits and questionnaires. The goal is to learn how the disease progresses over time to help prepare for future treatment trials.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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