Mitochondrial
Mitochondrial DNA-associated Leigh syndrome
2
studies recruiting now
as of 7 Sept 2026
2
studies registered in total
as of 7 Sept 2026
3
countries with a recruiting site
as of 7 Sept 2026
15 Feb 2013
most recent study posted
among recruiting studies
Recruiting trials
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
Showing the 2 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.
Search all Mitochondrial DNA-associated Leigh syndrome studiesWhere recruiting studies are running
Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Mitochondrial DNA-associated Leigh syndrome
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the genes involved (MT-ATP6, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND5).
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).