跳至主要内容
临床试验/JPRN-UMIN000026021
JPRN-UMIN000026021已完成4 期

Comparison between Optimal Coherence tomography guidance and Angiography Guidance in percutaneous coronary intervention - COCOA study

Wakayama Medical University0 个研究点目标入组 550 人开始时间: 2017年2月6日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
550

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 100years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients with ST elevation myocardial infarction(STEMI) 2) Hemodynamic supplements or vasopressors with cardiogenic shock (defined as persistent hypotension with systolic blood pressure <90mm/Hg persisting for more than 30 minutes) or pressure rising/intra-aortic balloon pumping at the time of the procedure Required patient 3) Heart failure patients 4) Patients with three branches disease 5) Patients planned to use bare metal stent (BMS) 6) Patients with renal dysfunction (eGFR 30ml/min/1.73m2 or less or serum creatinine 1.5mg/dl or more) 7) Patients during dialysis treatment 8) Patients who are known to have allergies to aspirin, clopidogrel, prasugrel, heparin, iodine contrast medium, 9) Patients with hemorrhagic complications such as intracranial hemorrhage and gastrointestinal bleeding 10) Patients planning surgical treatment with in 12month after PCI 11) Patients with one or more co-morbidities that shorten life expectancy to less than 12 months or that may interfere with the study process according to this study protocol 12) Patients participating in clinical trials of other medical devices and drugs and judged by the attending physician as affecting the main endpoint of this study 13) Patients scheduled to use IVUS for the PCI to be tested 14) Patients whose treatment subject lesion morphology falls under any of the following

研究者

相似试验