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Evaluation of the Next Generation WATCHMAN LAA Closure Technology in Non-Valvular AF Patients (EVOLVE) — EVOLVE  

Atrial Fibrillation Clinical Trial

Official title:
Evaluation of the Next Generation WATCHMAN LAA Closure Technology in Non-Valvular AF Patients

Clinical Trial Summary

This study will evaluate the next generation WATCHMAN Left Atrial Appendage (LAA) Closure Device as implanted in patients with non-valvular atrial fibrillation (AF) with a CHADS2 stroke risk stratification score of 1 or greater. This is a prospective, non-randomized study to evaluate the initial use of the next generation WATCHMAN Device.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01196897
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date May 2009
Completion date November 2013
View Details
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