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A Global Study Comparing Pulsed Field Ablation With Electrographic Flow Mapping Versus Posterior Wall Ablation for Persistent Atrial Fibrillation

Abroad (travel likely)Recruiting

Conditions

Atrial Fibrillation (AF) · Persistant Atrial Fibrillation

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

  • Grandview Medical Center, Birmingham, Alabama, United States

    Contact: Study coordinator (Susan Thorington) · susan.thorington@grandviewhealth.com
    Contact: Principal Investigator (Anil Rajendra)

  • Mercy Gilbert Medical Center, Gilbert, Arizona, United States

  • Banner University Medical Center, Phoenix, Arizona, United States

  • Arrhythmia Research Group, Jonesboro, Arkansas, United States

  • Alta Bates Summit Medical Center-Hospital, Oakland, California, United States

    Contact: Study coordinator (Milena Ferreira) · Milena.Ferreira@sutterhealth.org
    Contact: Principal Investigator (Steven Kang)

  • Stanford University Medical Center, Palo Alto, California, United States

    Contact: Study coordinator (Daniel Gonzalez) · danieljg@stanford.edu
    Contact: Principal Investigator (Tina Baykaner)

  • Pacific Heart Institute, Santa Monica, California, United States

  • St. Vincent's Medical Center, Jacksonville, Florida, United States

    Contact: Principal Investigator (Saumil Oza)

  • Piedmont Athens Regional, Athens, Georgia, United States

    Contact: Study coordinator (Heather Keperling) · Heather.keperling@piedmont.org
    Contact: Principal Investigator (Kent Nilsson)

  • Emory University Hospital, Atlanta, Georgia, United States

  • St. Luke's Boise Medical Center, Boise, Idaho, United States

  • Endeavor Hospital, Glenview, Illinois, United States

    Contact: Study coordinator (Marisa Durante) · marisa.durante@endeavorhealth.org
    Contact: Principal Investigator (Mark Metzl)

  • St. John's Hospital, Springfield, Illinois, United States

    Contact: Study coordinator (Lauren McNeil) · lmcneil@prairieresearch.com
    Contact: Principal Investigator (Ziad Issa)

  • Mercy Hospital Medical Center, West Des Moines, Iowa, United States

    Contact: Study coordinator (Teresa Coulson) · teresa.coulson@mercyoneiowa.org
    Contact: Principal Investigator (Pitayadet Jumrussirikul)

  • Baptist Health Lexington, Lexington, Kentucky, United States

  • Massachusetts General Hospital, Boston, Massachusetts, United States

    Contact: Study coordinator (Grace Ha)
    Contact: Principal Investigator (Moussa Mansour)

  • Beth Israel Deaconess Medical Center-Hospital, Boston, Massachusetts, United States

    Contact: Study coordinator (Jenifer Kaufman)
    Contact: Principal Investigator (Patricia Tung)

  • William Beaumont Hospital, Royal Oak, Michigan, United States

  • St. Mary's Duluth Clinic Regional Heart Center, Duluth, Minnesota, United States

    Contact: Study coordinator (Kaitlyn Tollerud)

  • Mount Sinai Medical Center, New York, New York, United States

  • Good Samaritan - Suffern, Suffern, New York, United States

  • Mission Hospital, Asheville, North Carolina, United States

  • Cleveland Clinic Foundation, Cleveland, Ohio, United States

  • Ohio State University Medical Center, Columbus, Ohio, United States

  • OhioHealth Research and Innovation Institute - Riverside Methodist Hospital, Columbus, Ohio, United States

    Contact: Study coordinator (Steven Neville) · Steven.Neville@ohiohealth.com
    Contact: Principal Investigator (Anish Amin)

  • Sacred Heart Medical Center at Riverbend, Springfield, Oregon, United States

  • Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

    Contact: Study coordinator (Mary Gnap) · mary.gnap@pennmedicine.upenn.edu
    Contact: Principal Investigator (David Callans)

  • Presbyterian University of Pennsylvania Medical Center, Pittsburgh, Pennsylvania, United States

  • University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

    Contact: Study coordinator (Melissa Enlow) · enlowms@upmc.edu
    Contact: Principal Investigator (Sandeep Jain)

  • Texas Cardiac Arrhythmia Research Foundation, Austin, Texas, United States

  • Christus Trinity Mother Frances Health System, Tyler, Texas, United States

  • Inova Fairfax Hospital, Falls Church, Virginia, United States

  • Sentara Norfolk General Hospital, Norfolk, Virginia, United States

    Contact: Study coordinator (Katherine Worcester) · ksworces@sentara.com
    Contact: Principal Investigator (Erich Kiehl)

  • AZORG, Aalst, Belgium

  • Hartcentrum Hasselt Jessa Ziekenhuis Campus Virga Jesse, Hasselt, Belgium

  • Centre Hôpital Universitaire Rouen, Hôpital Charles Nicolle, Rouen, France

  • MVZ CCB Frankfurt und Main-Taunus GbR, Frankfurt, Germany

    Contact: Study coordinator (Negin Azimi Hashemi) · n.azimi-hashemi@ccb.de
    Contact: Principal Investigator (Boris Schmidt)

  • Prince of Wales Hosptial, Shatin, Hong Kong, Hong Kong

  • St. Antonius Ziekenhuis, Nieuwegein, Netherlands

  • Erasmus MC - University Medical Center Rotterdam, Rotterdam, Netherlands

    Contact: Study coordinator (Elco van der Heide) · e.vanderheide@erasmusmc.nl
    Contact: Principal Investigator (Sing-Chien Yap)

  • Hospital Clinic de Barcelona, Barcelona, Catalonia, Spain

    Contact: Study coordinator (Judith Lara) · jlara@clinic.cat
    Contact: Principal Investigator (IVO Roca Luque)

  • Clinica Universidad de Navarra, Pamplona, Navarre, Spain

View source on ClinicalTrials.gov(opens in a new tab)