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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Tissue Sample Study for Mitochondrial DisordersBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cerebral Small Vessel Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Leber hereditary optic neuropathy, Leigh syndrome, MELAS syndrome, Nutritional and Metabolic Diseases, Pyruvate Metabolism, Inborn Errors, brain disorder, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inborn mitochondrial myopathy, metabolic disease, mitochondrial encephalomyopathy, mitochondrial neurogastrointestinal encephalomyopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease, vascular disorderEnrolling by invitationNot stated2026-01-07NCT01803906

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Research sitesCityCountryLinked trials
Columbia UniversityNew YorkUnited States154