NCT05504356Recruiting
Volunteers to Investigate Best Results for Ablation and Novel Therapies for Atrial Fibrillation
Source: ClinicalTrials.gov · Last updated 5 Oct 2026
Brief summary (registry, in English)
VIBRANT-AF seeks to: * Identify clinically relevant predictors of effectiveness and complications of AF ablation procedures in a prospective, US-based, multi-center, real-world longitudinal study * Assess changes in modifiable lifestyle-related exposures influence the effectiveness of AF ablation * Determine incidence and predictors of complications of AF ablation procedures Participants will connect with the Eureka Research Platform and answer a series of surveys and activities over a one-year period. They will be asked about lifestyle habits, recurrence of AFib, hospitalizations, and general feelings and emotions.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 1125 (estimated)
- First submitted
- 15 Aug 2022
- Start date
- Apr 2022
- Primary completion date
- Oct 2026
- Lead sponsor
- University of California, San Francisco
- Diseases
- Atrial fibrillation
- NCT number
- NCT05504356
What you commit to
- Study type: Observational
- Planned participants: 1125
- From Apr 2022 to the primary completion date, Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Unable to consent for themselves
- Unable to read, speak, comprehend English
Who the study is looking for
- Adults age 18 and older
- Must have a smartphone device (iOS and/or Android) and cell phone number to participate on the mobile app, and will be willing to download the Eureka Research Platform mobile application
- Must have email address to participate on the web portal (accessible on any web-connected device)
- Undergone a catheter ablation procedure for atrial fibrillation in the week prior to recruitment, or have an ablation planned for within a week from recruitment
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of California San Francisco Coordinator of this site? Confirm its status | San Francisco | United States | Recruiting |
Related publications
- Feasibility of Self-Reported Surveillance After Catheter Ablation for Atrial Fibrillation Using A Mobile Application.JACC Adv · 2026 · PMID 41906612
This page is information, not medical advice. Discuss any trial with your doctor.