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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Taiwan Associated Genetic and Nongenetic Small Vessel DiseaseBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cerebral Small Vessel Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fabry disease, HTRA1-related autosomal dominant cerebral small vessel disease, Infarction, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Necrosis, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, X-linked disease, brain disorder, brain infarction, brain ischemia, brain small vessel disease 1 with or without ocular anomalies, cardiovascular disorder, central nervous system disorder, cerebral arterial disease, cerebral infarction, cerebrovascular disorder, dementia, hereditary disease, inborn errors of metabolism, intracranial arterial disease, ischemic disease, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, sphingolipidosis, stroke disorder, vascular dementia, vascular disorderRecruitingNot stated2026-01-20NCT05473637