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The Brugada Syndrome: a Follow-up Study

Conditions
Brugada Syndrome
Registration Number
NCT03485508
Lead Sponsor
Universitair Ziekenhuis Brussel
Brief Summary

Although for many years the Brugada syndrome has been labelled as a purely electrical disease in the structurally normal heart, the evolution of imaging techniques has enabled the discovery of subtle morphofunctional alterations in some of the Brugada syndrome patients. We will use new echocardiographic techniques to assess cardiac function in these patients and new parameters will be evaluated for their prognostic value as risk stratificators.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
150
Inclusion Criteria
  • 18 years or older
  • Diagnosis of Brugada syndrome
Exclusion Criteria
  • history of pericarditis, ischemic heart disease, cardiomyopathy of any origin, structural heart disease, or any other channelopathy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Composed outcome of sudden cardiac death, appropriate ICD shock and witnessed ventricular fibrillation6 years

Sudden cardiac death is death occuring within 24 hours after being seen in a healthy status or within 1 hour after initiation of symptoms.

Secondary Outcome Measures
NameTimeMethod
Syncope6 years

Loss of consciousness

Trial Locations

Locations (1)

UZ Brussel

🇧🇪

Jette, Brussels, Belgium

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