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临床试验/NCT01063543
NCT01063543已完成不适用

Population Pharmacokinetics of Fondaparinux Administered at Prophylactic Doses After Major Orthopedic Surgery in Everyday Practice

Centre Hospitalier Universitaire de Saint Etienne8 个研究点 分布在 1 个国家目标入组 997 人开始时间: 2004年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
997
试验地点
8
主要终点
To determine an anti-Xa activity value which is predicted of a haemorrhage risk

研究概览

简要总结

Fondaparinux is a synthetic antithrombotic agent with specific anti-factor Xa activity. A population pharmacokinetic model of fondaparinux, based on data obtained in patients included in phase II/III trials, has been described. However, the validity of this model in everyday practice needed to be confirmed. This study was a multicenter, prospective cohort study in consecutive orthopedic patients treated with 2.5 mg of fondaparinux. Anti-Xa activities were recorded in 809 patients. Population parameters and inter-individual variability were estimated using NONMEM VI software. A two-compartment model with first-order absorption best described fondaparinux pharmacokinetics. Covariates partly explaining inter-individual variability were body weight, age and creatinine clearance estimated by the simplified Modification of Diet in Renal Disease formula. A body weight less than 50 kg and moderate renal failure increased drug exposure. These results suggest that fondaparinux pharmacokinetics need to be confirmed in patient populations not fully assessed in phase II/III studies

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patient who need leg major orthopedic surgery
  • age > 18 years
  • patient who need prophylactic doses of fondaparinux

排除标准

  • contra-indication to fondaparinux
  • renal insufficiency

结局指标

主要结局

To determine an anti-Xa activity value which is predicted of a haemorrhage risk

时间窗: day 9

次要结局

未报告次要终点

研究者

研究点 (8)

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