| Recruiting | N/A | 1500 | Europe, Canada, US | | Andrea Gropman, National Center for Research Resources (NCRR), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Rare Diseases Clinical Research Network | Brain Diseases, Metabolic, Inborn, Amino Acid Metabolism, Inborn Errors, Urea Cycle Disorders | 07/25 | 07/26 | | |
NCT05554835: Global Registry and Natural History Study for Mitochondrial Disorders |
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| Recruiting | N/A | 6000 | Europe | | LMU Klinikum, European Commission, German Federal Ministry of Education and Research, University of Pisa | 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 | 12/40 | 12/40 | | |
