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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 Young-hak Kim, MD
Email yhkim@amc.seoul.kr
Status Recruiting
Phase N/A
Start date September 2016
Completion date June 2021

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