ICM, Hôpital Pitié-Salpêtrière

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Evaluation of an Intensive Training Program for Patients with Hereditary Spastic Paraparesis SPG4/Spast	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, 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	Recruiting	Not applicable	2024-11-25		NCT06229626

Clinical trials