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临床试验/NCT02971111
NCT02971111已完成不适用

Evaluation of Thromboelastometry in Sepsis in Correlation to Bleeding During Invasive Procedures

University Hospital, Motol0 个研究点目标入组 76 人开始时间: 2013年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
76
主要终点
incidence of bleeding complications

研究概览

简要总结

The purpose of this study is to analyze occurence of bleeding complications during invasive procedures in septic patients with normal tromboelastometry results despite prolonged standard coagulation tests results

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
24 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • sepsis/septic shock
  • prolonged PT-INR (international normalized ratio) ≥ 1.3
  • normal ROTEM-EXTEM results.

排除标准

  • patients on antiplatelet drugs or anticoagulant therapy (heparin, vitamin K antagonists...)
  • patients with cirrhosis

结局指标

主要结局

incidence of bleeding complications

时间窗: 2013 - 2016

In our group of 76 septic patients who had normal values of EXTEM despite prolonged INR/PR invasive procedures were performed without severe bleeding.

次要结局

未报告次要终点

研究者

发起方
University Hospital, Motol
申办方类型
Other
责任方
Principal Investigator
主要研究者

Durila Miroslav MUDr. Ph.D.

clinical researcher

University Hospital, Motol

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