A Longitudinal Natural History Study of OPA1-Associated Autosomal-Dominant Optic Atrophy
A Longitudinal Natural History Study of OPA1-Associated Autosomal-Dominant Optic Atrophy
Recruiting · NCT07729982 · Registry updated 2026-07-28Clinical trials
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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 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Ludwig-Maximilians - University of Munich | 67 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Department of Ophthalmology, LMU University Hospital, LMU Medizin, Ludwig-Maximilians-Universität München | Munich | Germany | 1 |