Scientific Institute IRCCS E. Medea - Polo di Conegliano

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Observational Study to Observe Variations of Gait Parameters in Patients With Neuromuscular Diseases	Charcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, central nervous system disorder, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, motor neuron disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, spinal cord disorder, spinal muscular atrophy	Recruiting	Not stated	2026-01-20		NCT06666816

Clinical trials