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临床试验/JPRN-UMIN000018751
JPRN-UMIN000018751招募中未知

Acute phase intra-stent tissue reduction effect of prasugrel compared with clopidogrel in patient with acute coronary syndrome - Acute effect of parsugrel in ACS

Kobe University Graduate School of Medicine0 个研究点目标入组 100 人开始时间: 2015年8月21日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

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 who cannot give informed consent. 2. Absolute contraindications or allergy that cannot be pre-medicated to iodinated contrast or to any of the study medications including both prasgrel and clopidgrel. 3. Contraindications to angiography. 4. If it is known, pregnant or nursing mothers. 5. If it is known, a creatinine clearance <30 mL/min. 6. Previous enrolment in this study. 7. Randomisation or planned use of other investigational drugs or devices in this trial. 8. the opinion of the investigator would result in suboptimal imaging or excessive risk of complication from placement of an OCT catheter. 9. insufficient OCT image quality 10. stent thrombosis was developed before secondary OCT 11. cardiac arrest 12. PCI performed on the next day after PCI due to unstable hemodynamic status or chest pain 13. Curprit lesion located in (left main trunk or in )the ostial coronary artery or in a previous stent implantation(stent occulusion or stent restenosis) or in a saphenous vein graft ,in arterial bypass. 14. Stroke was developed after PCI 15. uncontrollable heart failure 16. active bleeding 17. active infection

研究者

发起方
Kobe University Graduate School of Medicine

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