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Clinical Trial Summary

Brugada syndrome (BrS) is the leading cause of sudden death in young Asian adults including Thailand. This syndrome may be hereditary and involve mutations in certain genes. Aim of the study is to identify the relationship between genetic variants and the diagnosis/clinical severity of patients with BrS.


Clinical Trial Description

This cohort study recruits BrS patients with confirmed Brugada type 1 ECG and healthy volunteers in Thailand. Data collection consists of demographic, clinical data, ECG and blood sample for genetic studies. Genotyping was done by whole genome sequencing and SNP array then compared between cases and controls. Each BrS patient will be followed up prospectively for symptoms and AICD shock. Subsequently, the study will analyze relationship between genetic variants and clinical data against clinical severity of BrS patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04232787
Study type Observational [Patient Registry]
Source Chulalongkorn University
Contact Apichai Khongphatthanayothin, MD
Phone 66891555545
Email apichaik@yahoo.com
Status Recruiting
Phase
Start date January 28, 2016
Completion date January 2023

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