Brugada syndrome

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Information
Disease name
Brugada syndrome
Disease ID
DOID:0050451
Description
"A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death." [url:http\://en.wikipedia.org/wiki/Brugada_syndrome]
Disease area statistics
Chromosome band
Gene symbol Chromosome Start Stop The number of variant
SCN5A 3 38,548,062 38,649,687 308
KCNH2 7 150,944,961 150,978,321 16
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT04257994 Active, not recruiting Distribution of Cell-cell Junction Proteins in Arrhythmic Disorders October 15, 2017 October 2025
NCT00702117 Completed Phase 4 Ajmaline Utilization in the Diagnosis and Treatment of Cardiac Arrhythmias June 2008 January 2010
NCT00292032 Completed Registry of Unexplained Cardiac Arrest May 2004 August 30, 2020
NCT02052765 Completed N/A AnalyST & Brugada Syndrome - Feasibility Study February 2011 May 2011
NCT02302274 Completed Diagnostic Value and Safety of Flecainide Infusion Test in Brugada Syndrome July 1, 2010 July 26, 2017
NCT02344277 Completed Evaluation of Subcutaneous Implantable Cardiac Defibrillator in Brugada Patients May 12, 2015 April 25, 2019
NCT02641431 Completed N/A Epicardial Ablation in Brugada Syndrome November 16, 2015 December 30, 2016
NCT03182777 Completed N/A Safety of Local Dental Anesthesia in Patients With Cardiac Channelopathies May 2015 August 2018
NCT03524079 Completed Right Ventricle Morphology and Hemodynamics in BrS April 19, 2018 November 9, 2019
NCT03992677 Completed Feasibility of Improving Risk Stratification in Brugada Syndrome December 1, 2017 August 1, 2022
NCT04124237 Completed Long Term Monitoring for Risk of Sudden Death May 15, 2015 August 30, 2020
NCT04420078 Completed Brugada Ablation of VF Substrate Ongoing MultiCenter Registry July 1, 2017 May 1, 2022
NCT04650009 Completed Physical Activity in Children With Inherited Cardiac Diseases May 1, 2020 February 1, 2021
NCT04712136 Completed N/A Healthy-related Quality of Life and Physical Activity of Children With Cardiac Malformations February 1, 2021 June 20, 2023
NCT06376552 Completed Artificial Intelligence for the Prioritization of Genetic Background in Brugada Syndrome December 19, 2018 June 6, 2022
NCT05048602 Recruiting Drug-induced Brugada Syndrome Research Database September 7, 2021 September 7, 2025
NCT03764592 Recruiting VF Mapping in Brugada and Early Repolarization Syndromes February 23, 2018 December 1, 2024
NCT03775954 Recruiting Fetal Electrophysiologic Abnormalities in High-Risk Pregnancies Associated With Fetal Demise July 1, 2018 April 30, 2024
NCT05274646 Recruiting Impact on Risk Stratification of Overlap Syndrome Phenotype in Patients With E1784K Mutation in SCN5A April 5, 2022 August 4, 2024
NCT05283759 Recruiting UZ Brussel HRMC Registry of Brugada Syndrome January 1, 1992 January 1, 2032
NCT02014961 Recruiting N/A Worm Study: Modifier Genes in Sudden Cardiac Death April 2015 April 2025
NCT05521451 Recruiting Clinical Cohort Study - TRUST March 17, 2021 December 31, 2031
NCT05643209 Recruiting N/A Brugada Syndrome Substrate Characterization and Ablation February 1, 2023 June 30, 2025
NCT05685134 Recruiting N/A Invasive and Clinical Features in Patients With Brugada Syndrome Undergoing Catheter Ablation November 3, 2020 June 2025
NCT02704416 Recruiting N/A Ablation in Brugada Syndrome for the Prevention of VF July 2016 July 2024
NCT00701077 Terminated Phase 3 DAPERB 3,4-DiAminoPyridine and Electrophysiological Response in Brugada Syndrome September 12, 2008 April 2010
NCT00927732 Terminated Phase 3 Hydroquinidine Versus Placebo in Patients With Brugada Syndrome February 2009 October 2014
NCT03485508 Unknown status The Brugada Syndrome: a Follow-up Study March 11, 2011 July 2019
NCT03491475 Unknown status Echocardiography During Ajmaline Test March 26, 2018 May 31, 2019
NCT04232787 Unknown status Southeast Asian Brugada Syndrome Cohort January 28, 2016 January 2023
NCT02933437 Unknown status Phase 2 The Response To Ajmaline Provocation in Healthy Subjects October 22, 2017 December 2019
NCT04580992 Unknown status Defining the Electrocardiographic Effect of Propofol on the Ajmaline Provocation Drug Challenge: A Prospective Trial November 16, 2020 October 31, 2022
NCT04808193 Unknown status N/A European Perioperative Brugada Survey March 31, 2021 December 31, 2021
NCT03435393 Unknown status Ripple Mapping for Epicardial Mapping of Brugada Syndrome September 1, 2017 September 2020
Disase is a (Disease Ontology)
DOID:10273
Cross Reference ID (Disease Ontology)
GARD:1030
Cross Reference ID (Disease Ontology)
ICD10CM:I49.8
Cross Reference ID (Disease Ontology)
MESH:D053840
Cross Reference ID (Disease Ontology)
MIM:PS601144
Cross Reference ID (Disease Ontology)
NCI:C142891
Cross Reference ID (Disease Ontology)
ORDO:130
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:418818005
Cross Reference ID (Disease Ontology)
UMLS_CUI:C1142166
Cross Reference ID (Disease Ontology)
UMLS_CUI:C1721096
Exact Synonym (Disease Ontology)
Bangungut
Exact Synonym (Disease Ontology)
Brugada type idiopathic ventricular fibrillation
Exact Synonym (Disease Ontology)
Dream disease
Exact Synonym (Disease Ontology)
Pokkuri death syndrome
Exact Synonym (Disease Ontology)
sudden unexplained nocturnal death syndrome
Exact Synonym (Disease Ontology)
SUNDS
OMIM Phenotype Series Number (OMIM)
PS601144
OrphaNumber from OrphaNet (Orphanet)
130
MeSH unique ID (MeSH (Medical Subject Headings))
D053840