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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Registry and Natural History Study for Early Onset Hereditary Spastic ParaplegiaCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, hereditary spastic paraplegia 11, hereditary spastic paraplegia 15, hereditary spastic paraplegia 3A, hereditary spastic paraplegia 4, hereditary spastic paraplegia 47, hereditary spastic paraplegia 50, hereditary spastic paraplegia 51, hereditary spastic paraplegia 52, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, palsy, paraplegia, peripheral nervous system disorder, polyneuropathyRecruitingNot stated2026-03-18NCT04712812