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Clinical Trial Summary

To establish the safety and efficacy of the commercially approved XIENCE Family Stent System (inclusive of XIENCE PRIME, XIENCE V, XIENCE Xpedition and XIENCE PRO [for use outside the United States [OUS] only]) in subjects with unprotected left main coronary artery disease by comparing to coronary artery bypass graft surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01205776
Study type Interventional
Source Abbott Medical Devices
Contact
Status Completed
Phase N/A
Start date September 29, 2010
Completion date June 28, 2019

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