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Clinical Trial Summary

To evaluate the safety and effectiveness of the 2.25 mm XIENCE V® Everolimus Eluting Coronary Stent System (XIENCE V® EECSS) in improving coronary luminal diameter in subjects with ischemic heart disease due to a maximum of two de novo native coronary artery lesions in small vessels, each in a different epicardial vessel.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00783796
Study type Interventional
Source Abbott Medical Devices
Contact
Status Terminated
Phase N/A
Start date October 2008
Completion date December 2013

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