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Southeast Asian Brugada Syndrome Cohort

NCT04232787 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2020-01-18

No results posted yet for this study

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.

Conditions

  • Brugada Syndrome

Sponsors & Collaborators

  • National Research Council of Thailand

    collaborator OTHER_GOV

  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    collaborator OTHER

  • Chulalongkorn University

    lead OTHER

Principal Investigators

  • Koonlawee Nademanee, MD · Chulalongkorn University

  • Yong Poovorawan, MD · Chulalongkorn University

  • Apichai Khongphatthanayothin, MD · Chulalongkorn University

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-28
Primary Completion
2021-01-31
Completion
2023-01-31

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04232787 on ClinicalTrials.gov