RecruitingNCT05554835

Global Registry and Natural History Study for Mitochondrial Disorders

◆ AI Clinical Summary

Plain-language summary for patients

Trial Parameters

ConditionMitochondrial Diseases

SponsorLMU Klinikum

Study TypeOBSERVATIONAL

PhaseN/A

Enrollment6,000

SexALL

Min AgeN/A

Max AgeN/A

Start Date2009-02-01

Completion2040-12

All 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

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Your Age

Your Sex

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * suspected or confirmed mitochondrial disease * willingness to participate Exclusion Criteria: * unwillingness to participate

Related Trials

NCT04322734

Transgenerational Metabolic-Immune Biomarkers of Neurological and Neurodevelopmental Disorders

View Trial →

NCT07450690

Exercise Training Effects on Muscle Function in Adults With Mitochondrial Myopathy

View Trial →

NCT06504433

The Natural History of Mitochondrial Diseases

View Trial →

VIEW ON CLINICALTRIALS.GOV ↗ MORE MITOCHONDRIAL DISEASES TRIALS