The CONFORM Pivotal Trial
Condition: Atrial Fibrillation · Stroke · Sponsor: Conformal Medical, Inc
About this study
The CLAAS® device will be evaluated for safety and efficacy by establishing its performance is non-inferior to the commercially available WATCHMAN® and Amulet™ left atrial appendage closure devices in patients with non-valvular atrial fibrillation. Patients who are eligible for the trial will be randomized to receive either the CLAAS device or the WATCHMAN or Amulet™ devices and will be followed for 5 years after device implant.
This description comes directly from the study's public registry record.
Talk to the study team
Sarah Gallagher · 952-270-8356 · sgallagher@conformalmedical.com
Always discuss trial participation with your own doctor first.
Locations (93)
| Grandview Medical Center | Birmingham, Alabama, United States | Recruiting |
| Banner University Medical Center Phoenix | Phoenix, Arizona, United States | Recruiting |
| Abrazo Arizona Heart Hospital | Phoenix, Arizona, United States | Active Not Recruiting |
| Arizona Heart Arrhythmia Associates | Phoenix, Arizona, United States | Recruiting |
| HonorHealth | Scottsdale, Arizona, United States | Recruiting |
| Pima Heart & Vascular | Tucson, Arizona, United States | Recruiting |
| St. Bernard's Medical Center | Jonesboro, Arkansas, United States | Recruiting |
| Loma Linda University Health | Loma Linda, California, United States | Recruiting |
| Huntington Hospital | Pasadena, California, United States | Recruiting |
| Pacific Heart Institute | Santa Monica, California, United States | Recruiting |
| Community Memorial Hospital Ventura | Ventura, California, United States | Recruiting |
| South Denver Cardiology Associates | Littleton, Colorado, United States | Recruiting |
+ 81 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT05147792