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RECRUITING
NCT07729982

A Longitudinal Natural History Study of OPA1-Associated Autosomal-Dominant Optic Atrophy

Sponsor: Ludwig-Maximilians - University of Munich

View on ClinicalTrials.gov

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