Evaluation of the WATCHMAN Left Atrial Appendage (LAA) Closure Device in Patients With Atrial Fibrillation Versus Long Term Warfarin Therapy
Status: | Completed |
---|---|
Conditions: | Atrial Fibrillation, Neurology |
Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 7/28/2018 |
Start Date: | November 2010 |
End Date: | November 2017 |
Prospective Randomized Evaluation of the WATCHMAN LAA Closure Device in Patients With Atrial Fibrillation (AF) Versus Long Term Warfarin Therapy
This was a prospective, randomized, multicenter study to provide additional information on
the safety and efficacy of the WATCHMAN LAA Closure Technology. The purpose of the PREVAIL
study was to confirm the efficacy endpoint as demonstrated in the PROTECT AF pivotal study
and to further demonstrate that the WATCHMAN LAA Closure Technology is safe and effective in
subjects with non-valvular atrial fibrillation who require anticoagulation therapy for
potential thrombus formation.
the safety and efficacy of the WATCHMAN LAA Closure Technology. The purpose of the PREVAIL
study was to confirm the efficacy endpoint as demonstrated in the PROTECT AF pivotal study
and to further demonstrate that the WATCHMAN LAA Closure Technology is safe and effective in
subjects with non-valvular atrial fibrillation who require anticoagulation therapy for
potential thrombus formation.
Key Inclusion Criteria:
- Paroxysmal, persistent or permanent non-valvular AF
- Eligible for long-term warfarin therapy
- Eligible to come off warfarin therapy
- Calculated CHADS2 score of 2 or greater. Also patients with a CHADS2 score of 1 may be
included if any of the following apply:
- Female age 75 or older
- Baseline LVEF ≥ 30 and < 35%
- Aged 65-74 and has diabetes or coronary artery disease
- Aged 65 or greater and has congestive heart failure
Key Exclusion Criteria:
- Contraindicated/allergic to aspirin
- Indicated for clopidogrel therapy or has taken clopidogrel within 7 days prior to
enrollment
- History of atrial septal repair or has an ASD/PFO device
- Implanted mechanical valve prosthesis
- NYHA Class IV CHF
- Resting heart rate > 110 bpm
- Participated previously in the PROTECT AF or CAP Registry studies
Key Echo Exclusion Criteria:
- LVEF < 30%
- Existing pericardial effusion > 2mm
- High risk PFO
- Significant mitral valve stenosis
- Complex atheroma with mobile plaque of the descending aorta and/or aortic arch
- Cardiac tumor
We found this trial at
41
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Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19104
(215) 662-4000
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