restrictive cardiomyopathy
restrictive cardiomyopathy
Explore linked clinical trials. Standard reference: MONDO:00052019 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Natural History Study in Pediatric Patients With MYBPC3 Mutation-associated Cardiomyopathy | Cardiomegaly, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, aortic valve disorder, aortic valve stenosis, cardiomyopathy, cardiovascular disorder, dilated cardiomyopathy, heart disorder, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, laminopathy, restrictive cardiomyopathy, subvalvular aortic stenosis | Active, not recruiting | Not stated | 2026-09-02 | NCT05112237 | |
| Pediatric Cardiomyopathy Mutation Analysis | Cardiomegaly, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypertrophy, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, cardiomyopathy, cardiovascular disorder, congenital heart disease, dilated cardiomyopathy, heart disorder, heart failure, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, laminopathy, left ventricular noncompaction, restrictive cardiomyopathy, subvalvular aortic stenosis | Recruiting | Not stated | 2026-06-22 | NCT02432092 | |
| National Network for Cardiovascular Genomics: Advancing Cardiovascular Healthcare for Hereditary Diseases in Brazil's Unified Health System Through a Multicenter Registry | Abnormalities, Multiple, Aneurysm, Aortic Dissection, Arrhythmias, Cardiac, Bone Diseases, Developmental, Brugada syndrome, Cardiac Conduction System Disease, Cardiomegaly, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Death, Death, Sudden, Death, Sudden, Cardiac, Dissection, Blood Vessel, Dyslipidemias, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Hemic and Lymphatic Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Loeys-Dietz syndrome, Marfan syndrome, Musculoskeletal Abnormalities, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Polymorphic Catecholaminergic Ventricular Tachycardia, Skin Abnormalities, Skin and Connective Tissue Diseases, Tachycardia, aortic aneurysm, aortic disorder, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, bone disorder, cardiac arrest, cardiomyopathy, cardiovascular disorder, congenital heart disease, connective tissue disorder, dilated cardiomyopathy, familial hypercholesterolemia, heart disorder, heart valve disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, hyperlipidemia, hyperlipoproteinemia, hypertrophic cardiomyopathy, inborn errors of metabolism, laminopathy, metabolic disease, musculoskeletal system disorder, non-compaction cardiomyopathy, restrictive cardiomyopathy, short QT syndrome, skin disorder, subvalvular aortic stenosis, vascular disorder, vascular hemostatic disease, ventricular tachycardia | Recruiting | Not stated | 2026-05-08 | NCT06546137 | |
| Early Identification and Treatment of Rare Cardiomyopathy Cohorts | Cardiomegaly, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, aortic valve disorder, aortic valve stenosis, cardiomyopathy, cardiovascular disorder, dilated cardiomyopathy, heart disorder, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, laminopathy, restrictive cardiomyopathy, subvalvular aortic stenosis | Not yet recruiting | Not applicable | 2025-01-27 | NCT06794710 | |
| AI-enabled Screening and Diagnosis of Cardiomyopathies Using Coronary CTA | Amyloid Neuropathies, Cardiomegaly, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, amyloidosis, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, cardiomyopathy, cardiovascular disorder, congenital heart disease, dilated cardiomyopathy, disease, familial amyloid neuropathy, heart disorder, heart valve disorder, hereditary amyloidosis, hereditary disease, hypertrophic cardiomyopathy, inborn errors of metabolism, inherited neurodegenerative disorder, laminopathy, metabolic disease, myocarditis, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, proteostasis deficiencies, restrictive cardiomyopathy, subvalvular aortic stenosis | Not yet recruiting | Not stated | 2024-12-27 | NCT06748261 | |
| Multimodal and Multidisciplinary Approach to Optimize Diagnostic, Prognostic, and Therapeutic Management of Patients with Non-ischemic Cardiomyopathies and Arrhythmogenic-inflammatory Phenotypes: a Multicenter, Observational, Retrospective and Prospective Registry Study. | Arrhythmias, Cardiac, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cardiac Complexes, Premature, Cardiac Conduction System Disease, Cardiomegaly, Cardiovascular Abnormalities, Cerebral Small Vessel Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, Death, Sudden, Cardiac, Fabry disease, Female Urogenital Diseases and Pregnancy Complications, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Pregnancy Complications, Cardiovascular, Tachycardia, Urogenital Diseases, Ventricular Premature Complexes, X-linked disease, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, brain disorder, cardiac arrest, cardiomyopathy, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, congenital heart disease, dilated cardiomyopathy, heart disorder, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, inborn errors of metabolism, laminopathy, left ventricular noncompaction, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, myocarditis, nervous system disorder, peripartum cardiomyopathy, pregnancy disorder, restrictive cardiomyopathy, sphingolipidosis, subvalvular aortic stenosis, vascular disorder, ventricular fibrillation, ventricular tachycardia | Recruiting | Not stated | 2024-09-23 | NCT06607471 | |
| Cardiac Amyloidosis Registry of University Hospital Leipzig | Amyloid Neuropathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, amyloidosis, cardiomyopathy, cardiovascular disorder, familial amyloid neuropathy, heart disorder, heart failure, hereditary amyloidosis, hereditary disease, inborn errors of metabolism, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, proteostasis deficiencies, restrictive cardiomyopathy | Recruiting | Not stated | 2023-11-13 | NCT06129656 | |
| Coronary Artery Disease and Coronary Microvascular Disease in Cardiomyopathies Registry | Angina Pectoris, Arterial Occlusive Diseases, Cardiomegaly, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypertrophy, Microvascular Angina, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, arteriosclerosis disorder, atherosclerosis, cardiomyopathy, cardiovascular disorder, coronary artery disorder, dilated cardiomyopathy, heart disorder, hereditary disease, ischemic disease, laminopathy, myocardial ischemia, restrictive cardiomyopathy, vascular disorder | Recruiting | Not stated | 2022-05-19 | NCT03479580 | |
| Sahlgrenska Cardiomyopathy Project | Cardiomegaly, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, amyloidosis, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, cardiomyopathy, cardiovascular disorder, congenital heart disease, dilated cardiomyopathy, giant cell myocarditis, heart disorder, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, laminopathy, metabolic disease, myocarditis, proteostasis deficiencies, restrictive cardiomyopathy, subvalvular aortic stenosis | Enrolling by invitation | Not stated | 2018-11-06 | NCT03527342 |