KCT0007397
Not yet recruiting
未知
Comparison between abluminal biodegradable polymer ultrathin sirolimus-eluting stent and durable-polymer everolimus-eluting stent (GENOSS randomized clinical trial)
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Samsung Medical Center
- Enrollment
- 850
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •? 19 years of age or older
- •? Patients diagnosed with stable coronary artery disease or acute coronary syndrome and with more than 50% coronary stenosis requiring stent insertion
- •? A person who can voluntarily sign the consent form
Exclusion Criteria
- •? If the following drugs are irritable or contraindicated (aspirin, clopidogrel, ticagrelor, prasugrel, heparin, sirolimus, or everolimus)
- •? a pregnant woman
- •? A person who is expected to have a life expectancy of less than one year due to non\-heart disease or less compliant with treatment (as determined by medical judgment by the investigator)
- •? Patients who refused to participate in the study
Outcomes
Primary Outcomes
Not specified
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