None listed
Conditions
Interventions
None listed
Sponsors
Seoul National University Bundang Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Adult subjects (aged 19 years or older) who have provided written informed consent to participate in the post-procedure registry.
Exclusion criteria
Exclusion criteria: - Vulnerable research subjects who are unable to give informed consent - Pregnant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Target lesion failure (cardiac death, non-fatal MI, Composite endpoint of target lesion revascularization) | — |
Secondary
| Measure | Time frame |
|---|---|
| ?Incidence of definite/probable stent thrombosis?Rates of the following clinical events: Death (cardiovascular, non-cardiovascular, undetermined), All-cause mortality All myocardial infarction All cerebrovascular events (ischemic or hemorrhagic), Target vessel revascularization and any revascularization, Bleeding (BARC bleeding score: 3a, 3b, 3c, 5)? Clinical and procedural success of the medical device | — |
Countries
Korea, Republic of
Contacts
Public ContactJINKYUNG GO
Seoul National University Bundang Hospital
Outcome results
None listed