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Clinical Trial Summary

The primary objective is to determine whether IVUS- (vs. OCT-) guided BVS implantation is non-inferior to achieve a large in-scaffold minimal lumen area (primary endpoint) measured by OCT at 1-year follow-up.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02814578
Study type Interventional
Source Asan Medical Center
Contact
Status Terminated
Phase N/A
Start date July 31, 2017
Completion date July 31, 2017

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