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Taking people in United StatesNo phase

Tracks adults with atrial fibrillation after heart rhythm ablation

Follows adults having ablation for atrial fibrillation, tracking habits and heart rhythm.

Plain-language title generated from the registry record
Registry title: Volunteers to Investigate Best Results for Ablation and Novel Therapies for Atrial Fibrillation

Key facts

Where
San Francisco, United StatesSee the site

Where in United States

  • University of California San FranciscoSan Francisco, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of California, San Francisco
Trial code
NCT05504356
Record updated
5 October 2026
Original description
VIBRANT-AF seeks to:Read full original descriptionShow less

Volunteers to Investigate Best Results for Ablation and Novel Therapies for Atrial Fibrillation

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.

Inclusion: 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.

Exclusion: Unable to consent for themselves; Unable to read, speak, comprehend English.

ClinicalTrials.gov NCT05504356