DCS versus DES for One-month DAPT in patients with ACS: ONE-PASS Trial
Not Applicable
Recruiting
- Conditions
- Diseases of the circulatory system
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 3520
Inclusion Criteria
1. Age =19 years
2. All subjects who are acceptable candidates for treatment with a DCS or DES because of ACS
3. Provision of informed consent
Exclusion Criteria
1. Current or potential pregnancy
2. Need of oral anticoagulation therapy
3. Inability to follow the patient over the period of 1 year after enrollment, as assessed by the investigator
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient-oriented composite endpoint (POCE): The composite of all-cause death, MI, or any revascularization
- Secondary Outcome Measures
Name Time Method Device-oriented composite endpoint (DOCE): The composite of cardiovascular death, MI (not clearly attributable to a non-target vessel), or clinically-driven target-lesion revascularization (TLR);All-cause death;Cardiovascular death;Myocardial infarction;Stroke;Stent thrombosis (definite or probable);Any revascularization;Target-vessel revascularization;Non-target vessel revascularization;Target-lesion revascularization;BARC type 2-5 bleeding;BARC type 3-5 bleeding