The CONFORM Pivotal Trial
Sponsored by 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.
Enrolling at this location
Henry Ford St. John Hospital
Detroit, Michigan
I'm interestedThis study also enrolls at 75 other locations. See all.
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Trial data sourced from ClinicalTrials.gov.