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临床试验/ACTRN12614000963628
ACTRN12614000963628已完成2 期

Major trauma patients with inferior vena cava filters versus no prophylaxis in preventing venous thromboembolism

Medical Research Foundation, Royal Perth Hospital0 个研究点目标入组 240 人开始时间: 2014年9月9日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
240

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Patients will be eligible for the trial (1) if they are considered to have contraindications to pharmacologic thromboprophylaxis within 72 hours of hospital admission by their attending trauma or neurosurgeons AND (2) Injury Severity Score >15.

排除标准

  • 1. Severe head or systemic injury where death within 48 to 72 hours is expected.
  • 2. Attending clinicians judge that patients are at low-risk of bleeding and can receive pharmacologic thromboprophylaxis within 3 days after major trauma.
  • 3. Patients who have CT evidence of pulmonary embolism on admission to the hospital after trauma.
  • 4. Patients who have been treated with full systemic anticoagulation by warfarin, UFH or LMWH for a pre-existing medical disease (e.g. patients with chronic atrial fibrillation requiring systemic anticoagulation) until admission due to trauma.
  • 5. Pregnant patients.
  • Specific contraindications to heparin or other form of pharmacologic thromboprophylaxis are listed below.
  • 1.Intracerebral haematoma or contusions
  • 2.Active bleeding on admission requiring more than 6 units of blood transfusion within the first 24 hours of admission after the injury
  • 3.Spinal cord injury resulting in neurological deficits or spinal cord haematoma is demonstrated in the MRI scan of the spine
  • 4.Complex pelvic fractures resulting in significant retroperitoneal haematoma
  • 5.Complex visceral organ injuries (e.g. splenic and liver lacerations) resulting in high risk of intraperitoneal bleeding
  • 6. Others, please specify

研究者

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