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Global Registry and Natural History Study for Mitochondrial Disorders

Study acronym: GENOMIT
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Study sites: 33 to 34v5
  2. Study sites: 18 to 33v4
  3. Re-verified, no change to tracked fieldsv3
  4. Study sites: 19 to 18v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05554835
Lead Sponsor LMU Klinikum
Collaborators: European Commission, German Federal Ministry of Education and Research, University of Pisa
Conditions
(from sponsor)		 Mitochondrial Diseases, Kearns-Sayre Syndrome, MIDD, SANDO, SCAE, NARP Syndrome, MELAS Syndrome, MERRF Syndrome +10 more
Related terms Ataxia Neuropathy Spectrum, Barth Syndrome, Coenzyme Q10 Deficiency, Kearns-Sayre Syndrome, Leigh Disease, MELAS Syndrome, MERRF Syndrome, Mitochondrial Diseases, Mitochondrial Myopathies, Neuropathy ataxia and retinitis pigmentosa, Ophthalmoplegia, Chronic Progressive External, VLCAD deficiency
Enrollment 6,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov