Coronary Artery Disease, Percutaneous Transluminal Coronary Angioplasty
Conditions
Keywords
coronary disease, drug eluting stent
Brief summary
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.
Detailed description
Consecutive patients receiving New DES without a mixture of other DES
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* coronary disease amenable to percutaneous coronary intervention (PCI) * no clinical and lesion limitations
Exclusion criteria
* patients with a mixture of several DES * terminal illness with life expectancy less than 1 year * patients with cardiogenic shock
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Composite of death, nonfatal myocardial infarction (MI), or ischemic-driven Target- Vessel Revascularization (TVR) | at 12 months post procedure |
Secondary
| Measure | Time frame |
|---|---|
| Death (all-cause and cardiac) | at 12 months and annually up to 5 years |
| Myocardial infarction | at 12 months and annually up to 5 years |
| Stent thrombosis | at 12 months and annually up to 5 years |
| Target-lesion and target-vessel revascularization | at 12 months and annually up to 5 years |
| Stroke | at 12 months and annually up to 5 years |
| Procedural success | at 1 day |
Countries
South Korea
Contacts
Asan Medical Center