Coronary Stenosis Clinical Trial
Official title:
A Multicenter, Randomized Trial to Compare 2 Link Nobori and 3 Link Xience Stents in Bifurcation Stenting
The primary objective of this study is to make a comparison of safety and efficacy of DESs
with different link number (2-link Nobori and 3-link Xience) in patients with de novo true
bifurcation lesions.
The minimum lumen diameter of the side branch ostium in bifurcation at 8 months and the MACE
rate until one year after PCI will be assessed in both groups.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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