Vascular responses to COMBO stent for acute coronary syndrome by Optical Coherence Tomography Assessment
Not Applicable
Recruiting
- Conditions
- The patients with acute coronary syndrome
- Registration Number
- JPRN-UMIN000039919
- Lead Sponsor
- ShonanKamakura general Hospital, Cardiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1) The patients with low ejection fraction (less than 20%). 2) The patients with recurrent myocardial infarction within 30 days. 3) The patients with fresh bleeding. 4) The patients with cerebral infarction within 6 months. 5) The patients with hemoglobin < 8.0 g/dl. 6) The patients with WBC <3000 or PLT < 100000. 7) The patients with positive HBV or HCV or HIV. 8) The patients with participate other clinical trial. 9, 10) The patients with pregnant women (including possible) or lactating women 11) The patients with renal failure (Cre>2.5 mg/dl) 12) The patients that research director judged inappropriate patients in this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint was that the degree of strut coverage which was evaluated by OCT at 1 month. Percentage of strut coverage was analyzed every 1 mm by OCT.
- Secondary Outcome Measures
Name Time Method