Motol University Hospital, Centre for Hereditary Ataxias

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Friedreich Ataxia Global Clinical Consortium UNIFIED Natural History Study	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Dyskinesias, Friedreich ataxia, Neurologic Manifestations, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Signs and Symptoms, Spinocerebellar Degenerations, atactic disorder, non-human animal, brain disorder, central nervous system disorder, cerebellar disorder, hereditary disease, inborn mitochondrial metabolism disorder, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, spinal cord disorder	Recruiting	Not stated	2026-09-01		NCT06016946

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