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Purpose of Study

To determine if left atrial appendage closure with the WATCHMAN FLX Device is a reasonable alternative to oral anticoagulation following percutaneous catheter ablation for non-valvular atrial fibrillation

Trial Status


Eligibility Criteria

Underwent a prior catheter ablation for non-valvular AF or planning to have a clinically indicated catheter ablation

Duration of Participation

Approximately 3 years

Contact Name: Jennifer Young, RN

Contact Phone: 515-633-3841

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