Major registry launches to map rare neurological disease
NCT ID NCT06572046
Summary
This study is creating a detailed patient registry for hereditary spastic paraplegia (HSP), a rare genetic condition that causes progressive leg stiffness and weakness. It will follow 500 patients over time at five Italian medical centers to better understand how the disease progresses in different people. The goal is to gather essential information that will help design future treatment trials, not to test a specific therapy.
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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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IRCCS Fondazione Stella Maris
RECRUITINGPisa, 56128, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Email: •••••@•••••
Conditions
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