Fabry Disease, Cardiac Variant
Fabry Disease, Cardiac Variant
Explore linked clinical trials. Standard reference: MESH:M05673623 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Long-Term Follow-up of Subjects Who Were Treated With ST-920 | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cerebral Small Vessel Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fabry Disease, Cardiac Variant, 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 disorder | Active, not recruiting | Not stated | 2026-08-20 | NCT05039866 | |
| CVI Alterations in FD: a Prospective, Multicenter, Observational Cohort Study | Fabry Disease, Cardiac Variant | Recruiting | Not stated | 2025-03-26 | NCT06512571 | |
| Evaluation of HEArt invoLvement in Patients With FABRY Disease | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cerebral Small Vessel Diseases, Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Fabry Disease, Cardiac Variant, Fabry disease, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Fibrosis, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Urogenital Diseases, X-linked disease, aortic valve disorder, aortic valve stenosis, brain disorder, cardiomyopathy, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, chronic renal failure syndrome, heart disorder, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, inborn errors of metabolism, kidney disorder, kidney failure, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, sphingolipidosis, stroke disorder, subvalvular aortic stenosis, urinary system disorder, vascular disorder | Recruiting | Not stated | 2022-07-07 | NCT03362164 |