Department of Ophthalmology, LMU University Hospital, LMU Medizin, Ludwig-Maximilians-Universität München

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Longitudinal Natural History Study of OPA1-Associated Autosomal-Dominant Optic Atrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, Optic Atrophy, Autosomal Dominant, cranial nerve neuropathy, eye disorder, hereditary disease, hereditary optic atrophy, inborn mitochondrial metabolism disorder, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, optic atrophy, optic nerve disorder	Recruiting	Not stated	2026-07-28		NCT07729982

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