IRCCS Eugenio Medea / Associazione la Nostra Famiglia

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Electroencephalogram in Patients With Friedreich's Ataxia for the Study of the Structural and Functional Connectome.	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Friedreich ataxia, Motor Disorders, Nutritional and Metabolic Diseases, Spinocerebellar Degenerations, brain disorder, central nervous system disorder, cerebellar disorder, hereditary disease, inborn mitochondrial metabolism disorder, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, psychiatric disorder, spinal cord disorder	Recruiting	Not applicable	2025-07-31		NCT07095062

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