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Clinical Trial Summary

The objective is to assess the effectiveness of permanent exclusion of the LAA with the LARIAT RS Suture Delivery Device and accessories in AF patients.


Clinical Trial Description

Prospective, observational, single-center, non-randomized study of a stand-alone procedure for the exclusion of the LAA with the LARIAT RS in patients with atrial fibrillation. Completed LAA exclusion will be assessed by TEE. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02059707
Study type Interventional
Source AtriCure, Inc.
Contact
Status Completed
Phase N/A
Start date January 2014
Completion date May 2015

See also
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Completed NCT01983605 - Left Atrial Appendage Exclusion Study N/A