Database for patients with drug-induced Brugada syndrome
Drug-induced Brugada Syndrome Research Database
This study is creating a database to gather information about patients with drug-induced Brugada syndrome to help understand their treatment and outcomes better.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | University of Campania Luigi Vanvitelli Academic / other |
| Locations | 1 site (Naples, Napoli) |
| Trial ID | NCT05048602 on ClinicalTrials.gov |
What this trial studies
This observational study aims to create a comprehensive database of patients diagnosed with drug-induced Brugada syndrome across participating centers. It will involve the systematic recording of patient characteristics, treatment approaches, and follow-up outcomes. The study will also evaluate prognostic factors related to clinically relevant endpoints to better understand the condition and its management.
Who should consider this trial
Good fit: Ideal candidates for this study are patients diagnosed with drug-induced Brugada syndrome.
Not a fit: Patients who do not have drug-induced Brugada syndrome or those unable to provide informed consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding and management of drug-induced Brugada syndrome, leading to improved patient outcomes.
How similar studies have performed: While there may be studies on Brugada syndrome, this specific focus on drug-induced cases is relatively novel and may not have extensive prior research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All consecutive patients with drug-induced Brugada Syndrome Exclusion Criteria: * Missing Informed Consent Form * Missing Contact Informations for Follow up
Where this trial is running
Naples, Napoli
- Vincenzo Russo — Naples, Napoli, Italy (Recruiting)
Study contacts
- Study coordinator: Vincenzo Russo, MD PhD
- Email: vincenzo.russo@unicampania.it
- Phone: +390817062355
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.