RECRUITING

Real-world Experience of Catheter Ablation for the Treatment of Paroxysmal and Persistent Atrial Fibrillation

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Conditions

Paroxysmal Atrial FibrillationPersistent Atrial Fibrillation

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The primary purpose of this registry is to obtain real-world clinical experience of Paroxysmal (PAF) and Persistent (PsAF) Atrial Fibrillation ablation radiofrequency (RF) technologies. Data from the registry will be used to assess clinical outcomes, including procedural efficiency, safety, and long-term, effectiveness of catheter ablation with novel RF technologies in PAF and PsAF patients.

Official Title

Real-world Experience of Catheter Ablation for the Treatment of Symptomatic ParoxysmaL and Persistent Atrial Fibrillation Using Novel CARTO Technologies: REAL AF Registry

Quick Facts

Study Start:2018-01-01
Study Completion:2027-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04088071

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Symptomatic Paroxysmal (AF episode terminate spontaneously within 7 days) or Persistent (AF sustained beyond 7 days) who, in the opinion of the investigator, are candidates for ablation for AF
  2. * 18 years of age or older
  3. * De Novo ablation procedure unless it is a repeat for a patient whose index procedure is also in the registry
  4. * Able and willing to participate in baseline and follow up evaluations for the full length of the registry
  5. * Willing and able to provide informed consent, if applicable
  1. * Enrolled in an investigational drug or device clinical trial, or any trial that dictates the treatment plan
  2. * Long-standing persistent AF (AF greater than one year's duration)
  3. * Having a repeat ablation, unless the subject's index ablation procedure is also included in the registry
  4. * In the opinion of the investigator, any known contraindication to an ablation procedure

Contacts and Locations

Study Contact

Kim Harbin
CONTACT
1-256-591-0727
kharbin@hrcrs.com
Jose Osorio, MD
CONTACT
josorio@hrcrs.com

Study Locations (Sites)

University of Alabama at Birmingham
Birmingham, Alabama, 35233
United States
Grandview Medical Center
Birmingham, Alabama, 35243
United States
Cardiology Associates of Mobile
Mobile, Alabama, 36695
United States
Valley Heart Rhythm Specialists
Chandler, Arizona, 85224
United States
Arrhythmia Research Group
Jonesboro, Arkansas, 72401
United States
Keck School of Medicine
Los Angeles, California, 90033
United States
Santa Barbara Cottage Hospital
Santa Barbara, California, 93105
United States
Community Memorial Hospital
Ventura, California, 93303
United States
University HealthCare Alliance
Walnut Creek, California, 94598
United States
The Medical Center of Aurora
Aurora, Colorado, 80012
United States
Ascension St. Vincent's
Jacksonville, Florida, 32204
United States
Naples Community Hospital
Naples, Florida, 34101
United States
Ascension Sacred Heart
Pensacola, Florida, 32504
United States
Sarasota Memorial Hospital
Sarasota, Florida, 34239
United States
Piedmont Healthcare
Atlanta, Georgia, 30309
United States
Memorial Health University Medical Center
Savannah, Georgia, 31404
United States
The Queen's Medical Center
Honolulu, Hawaii, 97813
United States
Northshore University Health System
Evanston, Illinois, 60201
United States
Prairie Education and Research
Springfield, Illinois, 62704
United States
Ascension St. Vincent's Hospital
Indianapolis, Indiana, 46260
United States
Norton Heart Specialists
Louisville, Kentucky, 40205
United States
Baptist Health Louisville
Saint Matthews, Kentucky, 40207
United States
Maine Medical Center
Portland, Maine, 04102
United States
Capitol CArdiology
Lanham, Maryland, 20706
United States
Brigham and Women's Hospital
Boston, Massachusetts, 02115
United States
McLaren Greater Lansing
Lansing, Michigan, 48910
United States
Sparrow Clinical Research
Lansing, Michigan, 48912
United States
Michigan Heart
Ypsilanti, Michigan, 48197
United States
Mississippi Baptist Medical Center
Jackson, Mississippi, 39202
United States
University of Missouri
Columbia, Missouri, 65212
United States
CoxHealth
Springfield, Missouri, 65807
United States
Cardiovascular Associates of the Delaware Valley
Haddon Heights, New Jersey, 08035
United States
Lovelace Health System
Albuquerque, New Mexico, 87102
United States
Mission Hospital
Asheville, North Carolina, 28801
United States
Novant Health Forsyth Medical Center
Winston-Salem, North Carolina, 27103
United States
University of Cincinnati
Cincinnati, Ohio, 45202
United States
The Christ Hospital
Cincinnati, Ohio, 45219
United States
Mount Carmel Columbus Cardiology Consultants
Columbus, Ohio, 43213
United States
Oklahoma Heart Hospital
Oklahoma City, Oklahoma, 73120
United States
Lancaster General Hospital
Lancaster, Pennsylvania, 17602
United States
University of Pennsylvania, Penn Presbyterian Medical Center
Philadelphia, Pennsylvania, 19104
United States
Allegheny Health Network
Pittsburgh, Pennsylvania, 15222
United States
WellSpan Health
York, Pennsylvania, 17403
United States
Upstate Cardiology
Greenville, South Carolina, 29607
United States
Carolina Cardiology Associates and OnSite Clinical Solutions
Rock Hill, South Carolina, 29732
United States
Medical City Dallas Hospital
Dallas, Texas, 75320
United States
St. Mark's Hospital
Salt Lake City, Utah, 84124
United States
Centra Health, Inc. dba Stroobants Cardiovascular Center
Lynchburg, Virginia, 24501
United States
Bon Secours St. Marys
Midlothian, Virginia, 23114
United States
MultiCare Institute for Research & Innovation
Tacoma, Washington, 98405
United States
MercyHealth
Janesville, Wisconsin, 53548
United States

Collaborators and Investigators

Sponsor: Heart Rhythm Clinical and Research Solutions, LLC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2018-01-01
Study Completion Date2027-12-31

Study Record Updates

Study Start Date2018-01-01
Study Completion Date2027-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Paroxysmal Atrial Fibrillation
  • Persistent Atrial Fibrillation