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临床试验/NCT01325779
NCT01325779撤回不适用

Prevention of Lower Extremity Deep Venous Thrombosis in the Surgical Intensive Care Unit: a Randomized Trial Comparing Subcutaneous Heparin and Subcutaneous Enoxaparin

Lisa Louwers1 个研究点 分布在 1 个国家开始时间: 2011年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
1
主要终点
Development of lower extremity deep venous thrombosis

研究概览

简要总结

Study hypothesis: Subcutaneous enoxaparin is more effective than subcutaneous heparin in preventing the development of DVT in the general surgical intensive care unit population.

Hospitalized patients are at increased risk for the development of blood clots in the legs, known as deep venous thrombosis (DVT). Surgical patients are in a higher risk category than the general hospital population due to a number of factors including undergoing surgery and increased risk of immobility. The highest risk patients are in the surgical intensive care unit, where their surgical risks for blood clots are combined with issues such as sepsis, acquired blood clotting disorders, and increasing age, each of which are factors that contribute to the risk of blood clot development. 1. Patients who develop these blood clots (DVTs) are at risk for chronic leg swelling, pain, and in some cases, chronic ulcer development on the leg. In the worst case scenario, these blood clots can break away and migrate to the lungs where they cause a pulmonary embolism (PE), a clot in the lungs that can cause significant breathing difficulty requiring intubation and mechanical ventilation, and in some cases, death.

According to recent research, DVTs account for over 200,000 patient deaths each year nationwide. 2. A large amount of data has supported the use of medication called heparin or enoxaparin in low doses to prevent these blood clots from forming while in the hospital. Both of these medications are considered standard of care for use patients considered moderate and high risk for the development of DVT. 3. While both of these medications have been shown to significantly reduce the occurrence of DVT in appropriate doses, 4. there has never been a direct comparison of the two medications in the highest-risk population of the surgical intensive care unit. Our own preliminary data suggests patients may have a lower incidence of DVTs with the use of enoxaparin versus heparin. Part of the reason for this may be the requirement for three times daily dosing of the heparin compared to once daily dosing for enoxaparin. There may also be some inherent differences in the efficacy of the medications themselves.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • age > 18 years old
  • admission to the surgical intensive care unit
  • admitting physician is a surgeon or patient is status-post a surgical procedure

排除标准

  • age < 18 years old
  • inability to obtain informed consent from patient or legal representative within 24 hours of SICU admission
  • patient admitted to neurosurgery or status-post a neurosurgical procedure
  • patient status-post an orthopedic procedure
  • patient admitted with a primary diagnosis of trauma
  • patient with a history of a bleeding disorder or other contraindication to even low-dose anticoagulation medicine including a history of heparin-induced thrombocytopenia verified with a positive serotonin-release assay or have a high clinical suspicion of new onset heparin-induced thrombocytopenia resulting in the discontinuation of heparin or enoxaparin by the treating physicians
  • patients on current full anticoagulation medications including a heparin drip or warfarin

研究组 & 干预措施

subcutaneous heparin

Active Comparator

干预措施: heparin (Drug)

subcutaneous enoxaparin

Active Comparator

干预措施: enoxaparin (Drug)

结局指标

主要结局

Development of lower extremity deep venous thrombosis

时间窗: hospital admission (day 1 ) to 3 months post discharge

次要结局

  • Adverse events associated with use of subcutaneous heparin and enoxaparin(hospital admission (day 1) through discharge)

研究者

发起方
Lisa Louwers
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Lisa Louwers

Principal Investigator

William Beaumont Hospitals

研究点 (1)

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