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临床试验/NL-OMON42991
NL-OMON42991已完成不适用

Acute coagulopathy and inflammation of trauma-3 - ACIT trial

Academisch Medisch Centrum0 个研究点目标入组 500 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
500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational invasive

入排标准

年龄范围
18 至 64(—)

入选标准

  • Age > 18 years
  • Sustained a blunt or penetrating trauma, with at least one of the following clinical parameters:
  • o Reparatory rate <10 or >25 times per minute
  • o Heart rate *120 per minute
  • o Systolic blood pressure < 90 mmHg
  • o Oxygen saturation <90%
  • o Estimated blood loss *500 mL
  • o GCS * 13 or abnormal pupil size and/or reaction
  • * Or clinical signs of at least one of the following diagnoses:
  • o 1 femur fracture
  • o Signs of flail thorax/pneumothorax/hematothorax or multiple rib fractures
  • o Signs of significant abdominal injury
  • o Pelvic fracture
  • o Spine injury

排除标准

  • Patients transferred from other hospitals
  • Patients presenting more than 120 minutes after time of injury
  • Patients who have received more than 2000 mL of intravenous fluids prior to emergency department arrival
  • Patients with burns >5% of their body surface area
  • Patients taking anticoagulant medication other than aspirin (<650mg/day)
  • Patients with a known bleeding diathesis
  • Patients with moderate to severe liver disease (Child's classification B or C)

研究者

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