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Clinical Trial Summary

The purpose of this study is to evaluate the performance of the Cardioblate Closure Device to occlude the LAA


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00841529
Study type Interventional
Source Medtronic Cardiovascular
Contact
Status Terminated
Phase Phase 2
Start date March 2009
Completion date June 2010

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