Paris Brain Institute ICM CRMR Neurogénétique, Hôpital de la Pitié-Salpêtrière Sorbonne Université UM75 Inserm U1127 CNRS UMR 7225 47 boulevard de l'Hôpital, CS21414

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
TreatHSP Platform: Adaptive Natural History Platform for Ataxias, HSPs, and Spastic Ataxias	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Disease Progression, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Spinocerebellar Degenerations, brain disorder, central nervous system disorder, central nervous system malformation, cerebellar disorder, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, spastic ataxia, spinal cord disorder	Recruiting	Not stated	2026-09-01		NCT07798674

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