Condition: Persistent Atrial Fibrillation · Longstanding Persistent Atrial Fibrillation · Sponsor: Medtronic Cardiac Surgery
The purpose of this study is to demonstrate the safety and effectiveness of the Cardioblate iRF and CryoFlex hand held devices for the treatment of non-paroxysmal atrial fibrillation (AF).
This description comes directly from the study's public registry record.
Stephanie Yong · 763-526-2032 · stephanie.yong@medtronic.com
Jessica Halverson · 763-514-9765 · Jessica.halverson@medtronic.com
Always discuss trial participation with your own doctor first.
| Stanford Hospitals and Clinic | Palo Alto, California, United States | Completed |
| Adventist Health St. Helena | St. Helena, California, United States | Withdrawn |
| Hartford Healthcare | Hartford, Connecticut, United States | Completed |
| St Vincent Heart Center of Indiana | Indianapolis, Indiana, United States | Recruiting |
| Massachusetts General Hospital | Boston, Massachusetts, United States | Recruiting |
| Corewell Health | Grand Rapids, Michigan, United States | Recruiting |
| Washington University School of Medicine | St Louis, Missouri, United States | Recruiting |
| ProMedica Toledo | Toledo, Ohio, United States | Completed |
| Allegheny General Hospital | Pittsburgh, Pennsylvania, United States | Recruiting |
| Lankenau Medical Center | Wynnewood, Pennsylvania, United States | Completed |
| Intermountain Medical Center | Murray, Utah, United States | Completed |
| Sentara Norfolk General Hospital | Norfolk, Virginia, United States | Completed |
+ 3 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT03546374