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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Characterization of Patients With Cardiomyopathy to Identify Critical Patients Candidates for Cardiac TransplantationAmyloid Neuropathies, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cardiomegaly, Cerebral Small Vessel Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, Death, Sudden, Cardiac, Fabry disease, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Muscular Disorders, Atrophic, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, X-linked disease, amyloidosis, aortic valve disorder, aortic valve stenosis, brain disorder, cardiac arrest, cardiomyopathy, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, dilated cardiomyopathy, disorder of glycogen metabolism, familial amyloid neuropathy, heart disorder, heart failure, heart valve disorder, hereditary amyloidosis, hereditary disease, hypertrophic cardiomyopathy, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inherited neurodegenerative disorder, laminopathy, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, proteostasis deficiencies, sphingolipidosis, subvalvular aortic stenosis, vascular disorderRecruitingNot stated2025-02-07NCT06813443
Italian Anderson Fabry Disease Cardiovascular RegistryBrain 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 disorderRecruitingNot stated2025-02-04NCT06806813