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A Longitudinal Natural History Study of OPA1-Associated Autosomal-Dominant Optic Atrophy
Sponsor: Ludwig-Maximilians - University of Munich
Summary
This prospective, monocenter, non-interventional observational study investigates the natural history as well as the clinical and genetic spectrum of OPA1-associated autosomal dominant optic atrophy. Participants will undergo standardized ophthalmic and functional assessments, including visual acuity testing, visual field testing, color vision and contrast sensitivity testing, optical coherence tomography, retinal flavoprotein fluorescence imaging, and video-oculography-based ocular motor and pupillary measurements. The study aims to characterize disease severity and progression over time and to identify structural, metabolic, and functional biomarkers that may serve as clinical endpoints for future therapeutic studies.
Official title: Clinical Characterisation of OPA1-Associated Autosomal-Dominant Optic Atrophy
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
50
Start Date
2026-07-16
Completion Date
2030-11
Last Updated
2026-07-28
Healthy Volunteers
No
Locations (1)
Department of Ophthalmology, LMU University Hospital, LMU Medizin, Ludwig-Maximilians-Universität München
Munich, Bavaria, Germany