Real-world Experience of Catheter Ablation for the Treatment of Arrhythmias
Recruiting now NCT04088071
Run by Heart Rhythm Clinical and Research Solutions, LLC · for 18 and older · All sexes
What this study is about
The primary purpose of this Registry is to assess procedural safety and long-term effectiveness of catheter ablations in the treatment of subjects with PAF, PsAF, and VA. The Registry will utilize real world clinical data obtained from the use of commercially available CARTO™ technologies under the authority of a health care practitioner within a legitimate practitioner-subject relationship. Data from the registry will be used to assess clinical outcomes, including procedural efficiency, safety, and long-term effectiveness of catheter ablation with novel technologies for arrhythmia patients.
Who can join (things the study team will check)
✅ You may be able to join if…
- Symptomatic PAF (AF episode terminate spontaneously within 7 days) or PsAF (AF sustained beyond 7 days, but less than 365 days) subjects who, in the opinion of the investigator, are candidates for catheter ablation.
- >18 years of age.
- Will be treated with Biosense Webster Inc. ablation technologies
- All AF ablations performed with BWI catheters are included. This includes repeat ablations where the index procedure was performed with a non-BWI catheter.
- Able and willing to participate in baseline and follow up evaluations
- Willing and able to provide informed consent, if applicable.
🚫 You may not be able to join if…
- Enrolled in an investigational drug or device clinical trial, or any trial that dictates the treatment plan
- Long-standing persistent AF (AF greater than one year)
- In the opinion of the investigator, any known contraindication to an ablation procedure CORE VA Cohort
✅ You may be able to join if…
- Documented ventricular arrhythmia appropriate for catheter ablation.
- >18 years of age.
- Will be treated with Biosense Webster Inc. ablation technologies
- Able and willing to participate in baseline and follow up evaluations
- Willing and able to provide informed consent, if applicable.
🚫 You may not be able to join if…
- Enrolled in an investigational drug or device clinical trial, or any trial that dictates the treatment plan.
- In the opinion of the investigator, any known contraindication to an ablation procedure.
Where this trial is running
- University of Alabama at Birmingham, Birmingham, Alabama, United States
- Grandview Medical Center, Birmingham, Alabama, United States
- Cardiology Associates of Mobile, Mobile, Alabama, United States
- Valley Heart Rhythm Specialists, Chandler, Arizona, United States
- Pima Heart and Vascular, Tucson, Arizona, United States
- Arrhythmia Research Group, Jonesboro, Arkansas, United States
- Keck School of Medicine, Los Angeles, California, United States
- Santa Barbara Cottage Hospital, Santa Barbara, California, United States
- Community Memorial Hospital, Ventura, California, United States
- University HealthCare Alliance, Walnut Creek, California, United States
- The Medical Center of Aurora, Aurora, Colorado, United States
- Colorado Heart and Vascular, Golden, Colorado, United States
+ 58 more sites.
Who to contact
Jennifer White, MS · 1-629-335-8261 · jwhite@hrcrs.com
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT04088071.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.