Scientists build database to unlock mysteries of rare childhood neurological disease
NCT ID NCT04712812
Summary
This study aims to gather detailed health information and biological samples from children and young adults (under 30) with early-onset hereditary spastic paraplegia (HSP), a group of rare genetic disorders that cause progressive stiffness and weakness in the legs. By tracking participants over time and creating a registry, researchers hope to better understand how the disease develops, identify targets for future therapies, and help design better clinical trials. The study does not test a treatment but seeks to build the knowledge needed for future breakthroughs.
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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
Email: •••••@•••••
Locations
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Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
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Conditions
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