Brugada syndrome
Brugada syndrome
Explore linked clinical trials. Standard reference: MONDO:001526315 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Prospective Multicentre Observational Registry of Peri-procedural Anaesthesia, Sedation and Related Medication Exposure in Patients With Brugada Syndrome | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathologic Processes, Pathological Conditions, Signs and Symptoms, cardiovascular disorder, heart disorder, hereditary disease | Recruiting | Not stated | 2026-09-08 | NCT07655102 | |
| Sudden Unexplained Death in Childhood (SUDC) Registry | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiovascular disorder, heart disorder, hereditary disease, sudden unexplained death in childhood | Recruiting | Not stated | 2026-08-28 | NCT03109197 | |
| 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 | |
| Distribution of Cell-cell Junction Proteins in Arrhythmic Disorders | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathologic Processes, Pathological Conditions, Signs and Symptoms, arrhythmogenic right ventricular cardiomyopathy, cardiomyopathy, cardiovascular disorder, congenital heart disease, heart disorder, hereditary disease | Recruiting | Not stated | 2026-05-08 | NCT04257994 | |
| Fetal Electrophysiologic Abnormalities in High-Risk Pregnancies Associated With Fetal Demise | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, Edema, Female Urogenital Diseases and Pregnancy Complications, Fetal Death, Fetal Diseases, Hemic and Lymphatic Diseases, Hernia, Hernia, Abdominal, Infant Death, Infant, Newborn, Diseases, Musculoskeletal Abnormalities, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Sudden Infant Death, Urogenital Diseases, alpha thalassemia spectrum, anemia, cardiovascular disorder, congenital heart disease, fetal erythroblastosis, gastroschisis, heart disorder, hematologic disorder, hereditary disease, hydrops fetalis, immune system disorder, inherited hemoglobinopathy, musculoskeletal system disorder, neonatal anemia, pregnancy disorder, pregnancy disorder with abortive outcome, thalassemia, twin to twin transfusion syndrome | Recruiting | Not stated | 2026-03-04 | NCT03775954 | |
| Analysis of the Presence and Cardiac Functional Effects of Anti-NaV1.5 Autoantibodies in Patients With Metastatic Tumors | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Digestive System Neoplasms, Neoplasms by Site, cardiovascular disorder, colonic disorder, colonic neoplasm, colorectal neoplasm, digestive system disorder, digestive system neoplasm, heart disorder, hereditary disease, intestinal disorder, malignant colon neoplasm, neoplasm | Not yet recruiting | Not applicable | 2026-01-23 | NCT07364656 | |
| Derivation of Human Induced Pluripotent Stem (iPS) Cells to Heritable Cardiac Arrhythmias | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Cardiomegaly, Cardiovascular Abnormalities, Channelopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Polymorphic Catecholaminergic Ventricular Tachycardia, Tachycardia, X-linked disease, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, cardiomyopathy, cardiovascular disorder, congenital heart disease, dilated cardiomyopathy, heart disorder, heart valve disorder, hereditary disease, hypertrophic cardiomyopathy, inherited neurodegenerative disorder, laminopathy, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease, subvalvular aortic stenosis, ventricular tachycardia | Enrolling by invitation | Not stated | 2026-01-16 | NCT02413450 | |
| Empagliflozin as a Potential Therapeutic Solution for Patients With Brugada Syndrome | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiovascular disorder, heart disorder, hereditary disease | Not yet recruiting | Phase 2 | 2025-09-12 | NCT07146880 | |
| Brugada Syndrome Substrate Characterization and Ablation | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiovascular disorder, heart disorder, hereditary disease | Recruiting | Not applicable | 2025-08-15 | NCT05643209 | |
| Unmasking Concealed Arrhythmia Syndromes | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiovascular disorder, heart disorder, hereditary disease | Recruiting | Not stated | 2025-05-23 | NCT06988189 | |
| GenLab: Unveiling the Genetic Landscape of Brugada Syndrome: Novel Biomarker Discovery for Precise Diagnosis | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiovascular disorder, heart disorder, hereditary disease | Recruiting | Not stated | 2025-05-14 | NCT06647927 | |
| Clinical Cohort Study - TRUST | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Polymorphic Catecholaminergic Ventricular Tachycardia, Tachycardia, Tachycardia, Supraventricular, arrhythmogenic right ventricular cardiomyopathy, atrial fibrillation, atrial flutter, atrial tachycardia, cardiomyopathy, cardiovascular disorder, congenital heart disease, heart disorder, hereditary disease, torsades de pointes, ventricular tachycardia | Recruiting | Not stated | 2025-03-30 | NCT05521451 | |
| DNA Methylation in Brugada Syndrome and Risk of Sudden Cardiac Death | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, Death, Sudden, Cardiac, Pathologic Processes, Pathological Conditions, Signs and Symptoms, cardiac arrest, cardiovascular disorder, heart disorder, hereditary disease | Not yet recruiting | Not stated | 2025-03-24 | NCT06888271 | |
| UZ Brussel HRMC Registry of Brugada Syndrome | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, cardiovascular disorder, heart disorder, hereditary disease | Recruiting | Not stated | 2022-03-17 | NCT05283759 | |
| China Inherited Ventricular Arrhythmias Registry | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Polymorphic Catecholaminergic Ventricular Tachycardia, Tachycardia, cardiovascular disorder, congenital heart disease, heart disorder, hereditary disease, short QT syndrome, ventricular tachycardia | Recruiting | Not stated | 2019-03-26 | NCT03880708 |