Champion-AF Study

Atrial Fibrillation
AGE: 18 years and older
SEX AT BIRTH: All
HEALTHY PARTICIPANTS: No
TYPE: Interventional Treatment Study
CONDITION: Atrial Fibrillation, Stroke
LOCATION: University Hospitals Cleveland Medical Center

Learn More About This Research Study

For more information, please contact study coordinator, Amy McKnight, RN, BSN, BCCV at 216-983-4896 and leave a message or complete the online form below.

Study Purpose

The purpose of this research study is to determine if left atrial appendage closure with the WATCHMAN FLX device is a reasonable alternative to non-vitamin K oral anticoagulants in patients with non-valvular atrial fibrillation.

Who Can Participate

Individuals who are 18 years and older and have documented non-valvular atrial fibrillation and has a calculated CHA2DS2-VASc score of 2 or greater for men and 3 or greater for women may be eligible for this study.

Request More Information

If you are 18 or older and would like to be contacted by a study team member for more information about this study, please provide your contact information below.

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