Six-Year quest to map rare nerve disease progression
NCT ID NCT05600764
Summary
This study aims to understand how symptoms change over time in people with a rare inherited nerve disorder caused by a TRPV4 gene mutation. Researchers will follow 70 patients for six years with annual visits to track muscle weakness, sensory problems, and daily function. The information gathered will help design future treatment trials for this condition.
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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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Johns Hopkins
RECRUITINGBaltimore, Maryland, 21287, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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