Registry for patients with Brugada Syndrome at UZ Brussel
UZ Brussel Heart Rhythm Management Center Monocentric Registry of Brugada Syndrome
This study is collecting information from patients with Brugada syndrome at UZ Brussel to better understand the condition and how it affects them and their families.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2000 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | Universitair Ziekenhuis Brussel Academic / other |
| Locations | 1 site (Brussels) |
| Trial ID | NCT05283759 on ClinicalTrials.gov |
What this trial studies
The UZ Brussel registry aims to collect comprehensive data on patients diagnosed with Brugada syndrome at the UZ Brussel hospital. This observational registry will gather demographic, clinical, and genetic information, as well as data from various heart imaging techniques. The goal is to create a detailed database that can help in understanding the condition and its implications for affected individuals and their families.
Who should consider this trial
Good fit: Ideal candidates for this registry are individuals diagnosed with Brugada syndrome.
Not a fit: Patients with conditions other than Brugada syndrome will not benefit from participation in this registry.
Why it matters
Potential benefit: If successful, this registry could enhance the understanding of Brugada syndrome and improve patient management strategies.
How similar studies have performed: While registries for specific conditions have been successful in the past, this particular approach is focused on Brugada syndrome and may provide novel insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Brugada syndrome diagnosis Exclusion Criteria: * Other diagnosis different from Brugada syndrome
Where this trial is running
Brussels
- UZ Brussel Heart Rhythm Management Center — Brussels, Belgium (Recruiting)
Study contacts
- Study coordinator: Carlo de Asmundis, MD, PhD
- Email: hrmc@uzbrussel.be
- Phone: +32024763704
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.