UZ Brussel HRMC Registry of Brugada Syndrome
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: No intervention because it is a patient registry.
- Who it may be relevant to
- Registry conditions: Brugada Syndrome. Basic parameters: 18 years — 100 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Belgium
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
UZ Brussel Heart Rhythm Management Center Monocentric Registry of Brugada Syndrome
Overview
The monocentric UZB registry for Brugada registry is intended to collect all data on patients affected by Brugada syndrome at UZ Brussel hospital (UZB).
Detailed description
The monocentric UZB registry for Brugada registry is intended to collect all data on patients affected by Brugada syndrome.
These includes:
1. demographical data: age, sex 2. antropometric data: height, weight, BMI 3. clinical data: comorbidities, arrhythmias, PM or ICD implantation, therapy
3\) data on the families: number of family members, sudden death history. 4) data on the genetics 5) data on: ECG, echocardiography, CT scan, MRI of heart, MRI of brain, ECG imaging, 3D electroanatomical mapping and ablation
Interventions
- Other No intervention because it is a patient registry
Primary outcome measures
- Ventricular arrhythmias [Time frame: through study completion, an average of 10 year]
- Atrial fibrillation [Time frame: through study completion, an average of 10 year]
- Death for any cause [Time frame: through study completion, an average of 10 year]
- Cardiovascular death [Time frame: through study completion, an average of 10 year]
- Genetic mutations [Time frame: Baseline]
Eligibility criteria
Inclusion criteria
- Brugada syndrome diagnosis
Exclusion criteria
- Other diagnosis different from Brugada syndrome
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Belgium · 1 center
- UZ Brussel Heart Rhythm Management Center — Brussels
Identifiers
NCT: NCT05283759 · UZ Brussel Brugada registry