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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
9
comparative method for BVS
The method of goldstandard for decision stent choice
Asan Medical Center
Seoul, Songpa-Gu, South Korea
Pusan National University Hospital
Pusan, South Korea
Ulsan University Hospital
Ulsan, South Korea
OCT-measured in-scaffold minimal lumen area
Time frame: 1 year
OCT-measured minimal scaffold area (MSA)
Time frame: 1 year
OCT-measured mean scaffold expansion
Time frame: 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.