# Natural History Study of FDXR Mutation-related Mitochondriopathy

> **NCT04580979** · — · COMPLETED · sponsor: **State University of New York at Buffalo** · enrollment: 33 (actual)

## Conditions studied

- Neurodegenerative Disease, Hereditary
- Mitochondrial Diseases
- Optic Atrophy

## Interventions

- **GENETIC:** Mutation analysis

## Key facts

- **NCT ID:** NCT04580979
- **Lead sponsor:** State University of New York at Buffalo
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2020-11-03
- **Primary completion:** 2023-08-17
- **Final completion:** 2023-08-17
- **Target enrollment:** 33 (ACTUAL)
- **Last updated:** 2024-03-08

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04580979

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04580979, "Natural History Study of FDXR Mutation-related Mitochondriopathy". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT04580979. Licensed CC0.

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