JPRN-UMIN000002940已完成未知
An association between post-treatment platelet reactivity and ischemic and bleeding events after stent implantation in patients with acute coronary syndromes: A multicenter, prospective, cohort study. - Platelet function monitoring in patients with acute coronary syndromes
Division of Cardiology, Yokohama City University Medical Center0 个研究点目标入组 360 人开始时间: 2010年1月4日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 360
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 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1) use of warfarin, ticlopidine, cilostazole, glycoprotein IIb/IIIa inhibitor, or fibrinolytics within 7 days before enrollment or duing study period. 2) serum hemoglobin level <10 g/dl or >18 g/dl 3) platelet count <100,000 /mm3 or >500,000 /mm3 4) hematologic or malignant disordor 5) major bleeding events within 7 days before enrollment 6) severe chronic renal failure (serum creatinine > 2mg/dl) 7) severe liver dysfunction (hepatic cirrhosis or portal hypertension) 8) acute coronary syndromes caused by stent thrombosis or in-stent restenosis 9) drug allergy of aspirin or clopidogrel 10) participating in the other trial (phase 1-3) 11) women of pregnant, childbearing potential or lactation 12) patients who are not allowed to participate in the trial by judgement of the treating physician
研究者
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