Assessment of neointimal coverage using two different imaging modalities at 2-week and 6-month after ultrathin vs thin strut drug-eluting stent implantation in coronary artery disease patients with ST elevation myocardial infarction -high-resolution angioscopy and OCT study
- Conditions
- Acute myocardial infarction
- Registration Number
- JPRN-UMIN000040642
- Lead Sponsor
- Aichi Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 110
Not provided
(1) Patients who cannot obtain written consent after oral consent by the patient or his/her legal representative (2) Patients with cardiogenic shock (3) Hemodialysis patients (4) Left main lesion / Bifurcation lesion requiring two stents / In-stent restenosis lesion (5) The target lesion is in the arterial bypass graft or saphenous vein bypass graft, or distal to the graft anastomosis site (6) Patients who are contraindicated for antiplatelet therapy or anticoagulant therapy (7) Patients who have difficulty in proper drug therapy (8) Patients who have a contraindication to contrast agents or have allergies to contrast agents (9) Patients scheduled for cardiac surgery within 6 months (10) Patients who have participated in another study and have not completed the observation period in that study (11) Patients who are judged to be unfavorable for participation in this study by the investigator and investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method