idiopathic cardiomyopathy
idiopathic cardiomyopathy
Explore linked clinical trials. Standard reference: MONDO:00051103 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Performance of the Cardiac Microcurrent (C-MIC) System With a Less Invasively Placed Left Ventricular Lead | Cardiomegaly, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiomyopathy, cardiovascular disorder, dilated cardiomyopathy, heart disorder, heart failure, hereditary disease, idiopathic cardiomyopathy, laminopathy | Recruiting | Not applicable | 2026-08-11 | NCT06920030 | |
| Precision Diagnosis and Risk Stratification of Rare Cardiomyopathies Based on Novel Cardiac Magnetic Resonance Techniques | Amyloid Neuropathies, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cardiovascular Abnormalities, Cerebral Small Vessel Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Danon disease, Fabry disease, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Musculoskeletal Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Noonan syndrome, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, X-linked disease, amyloidosis, brain disorder, cardiac sarcoidosis, cardiomyopathy, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, congenital heart disease, connective tissue disorder, disease, disorder of glycogen metabolism, familial amyloid neuropathy, heart disorder, hereditary amyloidosis, hereditary disease, idiopathic cardiomyopathy, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inherited neurodegenerative disorder, intellectual disability, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, proteostasis deficiencies, sphingolipidosis, vascular disorder | Recruiting | Not stated | 2026-01-21 | NCT07336394 | |
| Genomic Investigation of Cardiovascular Diseases | Arrhythmias, Cardiac, Arterial Occlusive Diseases, Infarction, Necrosis, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Ventricular Outflow Obstruction, aortic valve disorder, aortic valve stenosis, arteriosclerosis disorder, atrial fibrillation, cardiomyopathy, cardiovascular disorder, coronary artery disorder, heart disorder, heart valve disorder, idiopathic cardiomyopathy, ischemic disease, mitral valve insufficiency, myocardial infarction, myocardial ischemia, vascular disorder | Active, not recruiting | Not stated | 2025-01-16 | NCT00722748 |