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临床试验/NL-OMON47812
NL-OMON47812已完成不适用

Platelet reactivity and post-operative myocardial injury after major non-cardiac surgery (PROMISE). - PROMISE

Sint Antonius Ziekenhuis0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60

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
18 至 99(—)

入选标准

  • Patient must meet ALL of the following criteria:
  • * Males or females > 21 years of age and < 85 years
  • * Undergoing elective open abdominal vascular surgery
  • * On pre-operative ascal maintenance therapy

排除标准

  • 1) Patients who are unable to give informed consent or have life expectancy of < 1year
  • 2) Subjects who have received thrombolytic therapy within 24 hours or GpIIb/IIIa-inhibitors within last 30 days
  • 3) Subjects who had an acute coronary syndrome within the last 30 days
  • 4) Subjects with a contra-indication to anticoagulation or at increased bleeding risk
  • a. Past or present history (<1 year) of bleeding from gastrointestinal (haematemesis) melena, frank bleed in stool or visible haematuria
  • b. Known platelet count (<100,00/mm3 ) or coagulopathy or platelet disorder
  • c. History of major recent (<30 day) surgery or trauma
  • 5) Known Hb <6.5 mmol/L11g/dl or HCT <33%

研究者

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