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

> **NCT07729982** · — · RECRUITING · sponsor: **Ludwig-Maximilians - University of Munich** · enrollment: 50 (estimated)

## Conditions studied

- OPA1 Gene Mutation
- Optic Atrophy, Autosomal Dominant

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT07729982
- **Lead sponsor:** Ludwig-Maximilians - University of Munich
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2026-07-16
- **Primary completion:** 2030-10
- **Final completion:** 2030-11
- **Target enrollment:** 50 (ESTIMATED)
- **Last updated:** 2026-07-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07729982

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07729982, "A Longitudinal Natural History Study of OPA1-Associated Autosomal-Dominant Optic Atrophy". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07729982. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*