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临床试验/NCT00851864
NCT00851864已完成4 期

Weight-Adjusted Dosing of Tinzaparin in Pregnancy

University of Calgary1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2007年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
13
试验地点
1
主要终点
Rate of anti-Xa levels falling outside the target range of 0.4-1.2IU/mL

研究概览

简要总结

The purpose of this study is to evaluate the safety and efficacy of therapeutic anticoagulation with tinzaparin during pregnancy via weight-based dosing.

详细描述

Physicians in the Calgary Health Region are using tinzaparin (predominantly) and other low molecular weight heparins (LMWHs) for the treatment venous thromboembolism (VTE) in pregnancy. The most recent anticoagulation guidelines from American College of Chest Physicians (ACCP) suggest that heparin levels (anti-Factor-Xa activity levels) may be done periodically through pregnancy to determine the need to adjust the dose of LMWH as pregnancy progresses. This monitoring is widely practiced. There is no clear consensus in the literature, however, with some experts suggesting that initial and subsequent dosing may be done based on weight alone (as is done in the non-pregnant population). Given the multiple physiologic changes which occur to drug metabolism during pregnancy, this bears further evaluation. To date, there is very limited data on weight-adjusted dosing of LMWH in pregnancy. This study is therefore designed to determine if dosing of tinzaparin during pregnancy based on weight, with periodic weight-based adjustments, will result in adequate therapeutic anticoagulation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Singleton pregnancies in women over the age of 18 requiring anticoagulation for acute VTE (DVT/PE), or high-risk prophylaxis at a tinzaparin dose of 175 IU/kg.
  • High-risk patients include those with multiple (two or more) episodes of VTE and/or women receiving long-term anticoagulants (e.g. single event with known thrombophilia; APLAs and history of venous thrombosis)

排除标准

  • Multiple gestation\
  • Prosthetic valves
  • Active bleeding or other contraindication to anticoagulation therapy
  • Allergy to heparin, bisulfites, or fish, history of HIT (heparin induced thrombocytopenia), severe hypertension (diastolic >130)
  • Severe hepatic or renal failure
  • Patients over 100kg.

研究组 & 干预措施

A

Experimental

Women requiring therapeutic anticoagulation, singleton pregnancy,<30weeks

干预措施: Tinzaparin (Drug)

结局指标

主要结局

Rate of anti-Xa levels falling outside the target range of 0.4-1.2IU/mL

时间窗: anti-Xa level Day 1,28, then q4 weeks

次要结局

  • rate of clinical outcomes (PE/DVT) - objective testing of DVT/PE from radiology(1 year)
  • mean dosage requirement in each trimester(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Sue Ross

Adjunct Professor

University of Calgary

研究点 (1)

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