Purpose The TARGET All comers trial is a prospective, multicenter, randomized, two-arm, non-inferiority, open-label study with 1656 patients at 20 centers in Europe. The study is a "real world, all comers" study.
Primary objective: to compare the MicroPort Medical (Group) Co., Ltd Firehawk™cobalt chromium coronary stent ( rapamycin target eluting ) system with abluminal grooves containing a biodegradable polymer with the Abbott XIENCE family EES (Everolimus-Eluting stent) system with respect to cardiac death, myocardial infarction (not clearly attributable to a non-target vessel), Target Lesion Revascularization at 1 year in a "real world" patient population.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1,653
MicroPort Firehawk™ biodegradable polymer rapamycin target eluting stent
Abbott Xience family Everolimus-Eluting Stent
Rigshospitalet
Copenhagen, Denmark
Target Lesion Failure
Percentage of participants that had either Cardiac Death, Myocardial Infarction (not clearly attributable to a non-target vessel)or Target Lesion Revascularization (TLR, clinically indicated) after one year
Time frame: 12 months
In-stent late loss
In-stent late loss at 13 months post-procedure as measured by quantitative coronary angiography (QCA)
Time frame: 13 months
stent struth Neointimal thickness
stent struth Neointimal thickness at 3 months measured by Optical Coherence Tomography (OCT)
Time frame: 3 months
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