RP Cure Tracker

Trials / NCT05554835

Global Registry and Natural History Study for Mitochondrial Disorders

Recruiting now Observational Natural history / observational

Sponsor
LMU Klinikum
Treatment
Not listed
Gene
Not stated
Conditions
Mitochondrial Diseases, Kearns-Sayre Syndrome, MIDD, SANDO, SCAE, NARP Syndrome, MELAS Syndrome, MERRF Syndrome, Coenzyme Q10 Deficiency, LHON, MNGIE, MIRAS, Barth Syndrome, MDS, Mitochondrial Myopathies, Leigh Syndrome, Pearson Syndrome, CPEO
Ages
Any to no upper limit
Enrollment
6000 participants
Started
2009-02-01
Main results expected
2040-12
Results posted
Not yet
Record last updated
2026-08-07

What the study is testing

The main goal of the project is provision of a global registry for mitochondrial disorders to harmonize previous national registries, enable world-wide participation and facilitate natural history studies, definition of outcome measures and conduction of clinical trials.

Where it runs

Austria (2)
Germany (16)
Italy (16)

Open on ClinicalTrials.gov for contacts and eligibility