跳至主要内容
临床试验/EUCTR2011-004139-29-AT
EUCTR2011-004139-29-AT进行中(未招募)不适用

RETIC trial: Reversal of Trauma Induced Coagulopathy by using Coagulation factor concentrates or Fresh frozen Plasma

Medizinische Universität Innsbruck / UK für Anästhesie und Intensivmedizin & UK für Allgem. u. Chirurg. Intensivmedizin0 个研究点开始时间: 2011年11月9日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • I.1. Male and female subjects ? 18 years and < 80 years
  • I.2. Major trauma (ISS>15)
  • I.3. Clinical signs of ongoing bleeding or patients who are at risk for significant haemorrhage assessed and judged by the ED team in charge of patient
  • I.4. Presence of coagulopathy defined by ROTEM assays as follows,
  • o Patients with concomitant decreased fibrinogen polymerisation (ROTEM® FibTEM A10 of <7 mm after 10 min)
  • o Patients with concomitant decreased coagulation factor levels (ROTEM® ExTEM CT of >90 sec)
  • 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 180
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • E.1. Lethal injury
  • E.2. CPR on the scene,
  • E.3. Isolated brain injury, burn injury
  • E.4. Avalanche injury
  • E.5. Administration of FFP or coagulation factor concentrates before ED admission
  • E.6. Delayed (>6hours after trauma) admittance to ED
  • E.7. Known use of oral anticoagulants, or platelet aggregation inhibitors within 5 days before injury
  • E.8. Known history of severe allergic reaction to plasma products
  • E.9. Known history of congenital hemostasis disturbance, IgA or Protein C deficiency
  • E.10.Patients with a history of thromboembolic events or heparin induced thrombocytopenia (HIT) type 2 within the last year
  • E. 11. Patients with a body weight <45kg and >150kg
  • E.12. Patients that are known to be pregnant
  • E.13. Jehova‘s Witness
  • E.14. known participation in another clinical trial
  • E.15. Patient with known refusal of a participation in this clinical trial

研究者

发起方
Medizinische Universität Innsbruck / UK für Anästhesie und Intensivmedizin & UK für Allgem. u. Chirurg. Intensivmedizin

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