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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study of Migalastat in Pediatric Subjects (2 to <12 Yrs) With Fabry Disease and Amenable GLA VariantsBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cerebral Small Vessel Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fabry disease, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, X-linked disease, brain disorder, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, hereditary disease, inborn errors of metabolism, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, sphingolipidosis, vascular disorderRecruitingPhase 32026-09-01NCT06904261
Anatomy-based Fitting in Cochear Implant UsersCochlear Implant; Outcomes; Quality of LifeRecruitingNot applicable2025-08-12NCT05360212
Analysis of Musical and Voice Skills in Children and Adult Cochlear Implant UsersCochlear Implant; Music; VoiceRecruitingNot stated2025-08-12NCT05319678
Abbott Vascular Medical Device RegistryBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, X-linked disease, acute myocardial infarction, brain disorder, cardiovascular disorder, central nervous system disorder, coronary artery disorder, coronary restenosis, coronary stenosis, heart disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, myocardial ischemia, nervous system disorder, ornithine carbamoyltransferase deficiency, urea cycle disorder, vascular disorderRecruitingNot stated2025-07-03NCT04573660