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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History and Advanced Genetic Study of Pyruvate Dehydrogenase Complex DeficienciesBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Pyruvate Dehydrogenase Complex Deficiency Disease, Pyruvate Metabolism, Inborn Errors, X-linked disease, brain disorder, central nervous system disorder, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inherited neurodegenerative disorder, intellectual disability, metabolic disease, nervous system disorderRecruitingNot stated2026-10-05NCT03056794

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Research sitesCityCountryLinked trials
University of PittsburghPittsburghUnited States38