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临床试验/EUCTR2018-001867-22-ES
EUCTR2018-001867-22-ES进行中(未招募)1 期

TRANSFUSION OF RED BLOOD CELLS, TRANEXAMIC ACID AND FIBRINOGEN CONCENTRATE FOR SEVERE TRAUMA HEMORRHAGE AT PRE-HOSPITAL PHASE OF CARE. A PILOT TRIAL. - PRETIC

Banc de Sang i teixits0 个研究点目标入组 60 人开始时间: 2018年8月10日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
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
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • oAge =18 years AND
  • oPatients with severe trauma categorized as priority 0 or 1 according to the CatSalut Polytrauma Code (PPT) AND
  • oEvidence of bleeding or a high bleeding suspicion according to physician judgment OR
  • oPredicted to need transfusion according to TICCS score > 10.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 30
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 30

排除标准

  • oMoribund patient with devastating injuries and expected to die within 1-hour OR
  • oKnown objection to blood components transfusion OR
  • oKnown acquired or congenital coagulopathies not related to the actual trauma OR
  • oKnown anticoagulant treatment (vitamin K antagonist, dabigatran, rivaroxaban, apixaban) OR
  • oKnown Pregnancy OR
  • oSevere isolated traumatic brain injury OR
  • oHemorrhage not related to the actual trauma.

研究者

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