Actively Recruiting

Age: 18Years - 100Years
All Genders
ID05283759

UZ Brussel Heart Rhythm Management Center Monocentric Registry of Brugada Syndrome

Led by Universitair Ziekenhuis Brussel · Updated on 2022-03-17

2000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are collecting detailed information on patients diagnosed with Brugada syndrome at UZ Brussel hospital. The goal is to gather comprehensive data including demographics, clinical history, family history, genetic information, and results from various heart and brain imaging tests. This observational registry aims to understand the condition better over time. Participants' data will include age, sex, height, weight, body mass index, comorbidities, arrhythmias history, and device implantations like pacemakers or defibrillators. Family history including sudden death incidents, genetic mutation data, and diagnostic imaging such as ECG, echocardiography, CT scans, MRI of the heart and brain, ECG imaging, and 3D electroanatomical mapping will also be collected. Participants will be monitored for outcomes including ventricular arrhythmias, atrial fibrillation, overall death, cardiovascular death, and genetic mutations. These outcomes will be tracked throughout the study, averaging 10 years of follow-up. No active intervention is given as this is a patient registry. The study collects comprehensive long-term observational data to improve understanding of Brugada syndrome.

CONDITIONS

Brief Title

UZ Brussel HRMC Registry of Brugada Syndrome

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Brugada syndrome
Not Eligible

You will not qualify if you...

  • Diagnosis other than Brugada syndrome

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 10 years

Participants are observed with long-term data collection on heart rhythm and related health outcomes.

Periodic visits as needed for data collection and assessments

Trial Site Locations

Total: 1 location

1

UZ Brussel Heart Rhythm Management Center

Brussels, Belgium, 1090

Actively Recruiting

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Research Team

C

Carlo de Asmundis, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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