Atrial Fibrillation Ablation Registry
AFib
1 other identifier
observational
5,000
1 country
1
Brief Summary
The Atrial Fibrillation Ablation Registry (AFib Ablation Registry™) is designed to assess the prevalence, demographics, management, and outcomes of patients undergoing percutaneous catheter ablation procedures to treat atrial fibrillation (AF).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2019
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 20, 2019
CompletedFirst Submitted
Initial submission to the registry
August 8, 2019
CompletedFirst Posted
Study publicly available on registry
August 14, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 20, 2025
CompletedFebruary 28, 2023
February 1, 2023
6 years
August 8, 2019
February 27, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Unsuccessful treatment rate
measured by the number of repeated procedure
1 year
Secondary Outcomes (1)
Adverse Events
1 year
Interventions
A procedure used to treat an irregular heart rhythm (arrhythmia)
Eligibility Criteria
Adult patients, 18 years and older, undergoing percutaneous catheter ablation procedures to treat atrial fibrillation
You may qualify if:
- Adult patients
- years and older
- Undergoing percutaneous catheter ablation procedures to treat atrial fibrillation
You may not qualify if:
- \. none
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hoah Memorial Hospital Presbyterian
Newport Beach, California, 92663, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Leila Andres
Hoag Memorial Hospital Presbyterian
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- OTHER
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Data Coordinator
Study Record Dates
First Submitted
August 8, 2019
First Posted
August 14, 2019
Study Start
May 20, 2019
Primary Completion
May 20, 2025
Study Completion
May 20, 2025
Last Updated
February 28, 2023
Record last verified: 2023-02
Data Sharing
- IPD Sharing
- Will not share