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Global Registry and Natural History Study for Mitochondrial Disorders

NCT05554835 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 6000

Last updated 2025-06-05

No results posted yet for this study

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.

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

Sponsors & Collaborators

  • European Commission

    collaborator OTHER

  • German Federal Ministry of Education and Research

    collaborator OTHER_GOV

  • University of Pisa

    collaborator OTHER

  • LMU Klinikum

    lead OTHER

Principal Investigators

  • Thomas Klopstock, Prof. Dr. · LMU Klinikum, Munich

  • Michelangelo Mancuso, Prof. Dr. · Università di Pisa

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-01
Primary Completion
2040-12-31
Completion
2040-12-31

Countries

  • Austria
  • Germany
  • Italy

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05554835 on ClinicalTrials.gov