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临床试验/NCT01707732
NCT01707732已完成3 期

Adjusted Value of Thromboprophylaxis in Hospitalized Obese Patients: A Comparative Study of Two Regimens of Enoxaparin

University Hospital, Rouen1 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2012年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
92
试验地点
1
主要终点
Evaluate the anti- Xa activity between a standard treatment by Enoxaparin (40mg/ day) and an adapted dose of enoxaparin (60 mg/day) for thromboprophylaxis in obese patients hospitalized

研究概览

简要总结

Venous thromboembolism (VTE), deep vein thrombosis (DVT) or pulmonary embolism (PE) is a common medical condition encountered during hospitalization in a medical environment. The use of thromboprophylaxis with Low Molecular Weight Heparin (LMWH) or fondaparinux has reduced more than 50% relative risk of thromboembolic complications.However, while obesity defined by a body mass index (BMI) greater than 30 kg/m2, is a major risk factor for venous thrombotic events, data on obese patients are limited. In fact, less than 20% of patients included in the three major studies of preventive medicine had a BMI ≥ 30 kg/m2 and most studies specific to the obese population comes from a series of bariatric surgery patients or orthopedic surgery. The main results of this series show regarding the obese population a decrease of the anti-Xa activity during the administration of a standard dose of enoxaparin (40 mg / d). However, no specific recommendation in this population has not been published to date and therefore,the dosages currently used are the same regardless of the patient's weight. In this context, the use in obese patients hospitalized in a medical environment a stronger dosage of enoxaparin (60 mg / d) compared to the standard dose of 40 mg / day, could get rates anti-Xa activity levels more consistent with the treatment required, and thus reduce the risk for thromboembolic complications in these patients

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

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

  • Patient aged ≥ 18 ans.
  • Signed inform consent
  • Obesity defined by a BMI value ≥ 30 kg/m
  • Hospitalized for :
  • acute medical affection such as :
  • congestive heart failure (stage III or IV NYHA),
  • severe respiratory disease,
  • Infectious disease or acute rheumatologic disorder or inflammatory bowel disease with one or more additional risk factors, including active cancer, previous VTE, age > 75 y-o, estrogen therapy, chronic heart failure or chronic respiratory disease
  • or recent myocardial infarction(< 6 weeks), recent stroke with hemiparesis (< 15 days), previous VTE, myeloproliferative syndrome associated with one or more additional risk previously cited.
  • Affiliation to a welfare system.

排除标准

  • Subjects unwilling or unable to comply with study procedures
  • History of hypersensitivity to enoxaparin heparin induced thrombocytopenia
  • Previous history of heparin induced thrombopenia
  • acquired or inherited bleeding diathesis or coagulopathy,
  • Platelet count < 50.000 G/L,
  • History of clinically significant bleeding
  • Severe renal insufficiency with CrCl <30 ml/min (Cockcroft method),
  • Pregnancy or breastfeeding
  • Women without contraceptive methods
  • Severe peripheral arterial disease (Ankle blood pressure <50mm Hg)
  • Concomitant anticoagulant therapy
  • Severe psychiatric disease
  • History of disease or psychological or sensory anomaly susceptible to prevent the subject to understand indeed the conditions required for his participation to the protocol or preventing him from giving its enlightened consent
  • Person deprived of liberty by an administrative or judicial decision, or person under legal guardianship person
  • Patient participating to a trial or having participated in another medicinal trial within 1 month

研究组 & 干预措施

Enoxaparin 40mg/ day

Active Comparator

Enoxaparin administrated at the following dose : 40mg/ day

干预措施: Enoxaparin (Drug)

Enoxaparin 60 mg/day

Experimental

Enoxaparin administrated at the following dose : 60 mg/day

干预措施: Enoxaparin (Drug)

结局指标

主要结局

Evaluate the anti- Xa activity between a standard treatment by Enoxaparin (40mg/ day) and an adapted dose of enoxaparin (60 mg/day) for thromboprophylaxis in obese patients hospitalized

时间窗: 3 hours after third Eoxaparin injection

次要结局

  • Compare the occurrence of symptomatic venous thrombosis (deep venous thrombosis or pulmonary embolism) and the relevant bleeding events according to the enoxaparin treatments(All along the study (max 14 days))

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (1)

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