Global Registry and Natural History Study for Mitochondrial Disorders

ConditionsMitochondrial 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

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexAll

AgeNot listed

SponsorLMU Klinikum

About this trial

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

Qualifiers

suspected or confirmed mitochondrial disease

willingness to participate

Disqualifiers

unwillingness to participate

Trial design

Treatments tested in this trial

Not listed

Trial groups

6,000 Participants

are grouped into 1 trial group

Locations

Austria

Medical University Innsbruck, Department of Pediatrics6020, Innsbruck Austria

Salzburger Landeskliniken, SALK, Paracelsus Medizinische Privatuniversität5020, Salzburg Austria

Germany

Department of neurology, Klinikum rechts der Isar, Technical University Munich81675, MunichBavaria, Germany

Charité Virchow Klinikum, Klinik für Pädiatrie m. S. Neurologie13353, Berlin Germany

Sponsors and collaborators

LMU Klinikum

Lead sponsor

European Commission

Collaborator

German Federal Ministry of Education and Research

Collaborator

University of Pisa

Collaborator

Source ClinicalTrials.gov