About this trial
The objective of this study is to evaluate effectiveness and safety of the new drug-eluting stent (DES), as compared with the first-,second-,third-, and fourth-generation DES, in the "real world" daily practice.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
coronary disease amenable to percutaneous coronary intervention (PCI)
no clinical and lesion limitations
Disqualifiers
patients with a mixture of several DES
terminal illness with life expectancy less than 1 year
patients with cardiogenic shock
Trial population
consecutive patients amenable to PCI
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
27
Trial groupsSee each trial group below.
Trial outcomes
Primary outcomes
Composite of death, nonfatal myocardial infarction (MI), or ischemic-driven Target- Vessel Revascularization (TVR)
Secondary outcomes
Death (all-cause and cardiac)
Myocardial infarction
Stent thrombosis
Target-lesion and target-vessel revascularization
Locations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Seung-Jung Park
Lead sponsor
CardioVascular Research Foundation, Korea
Sponsor institution
CardioVascular Research Foundation, Korea
Collaborator