跳至主要内容
临床试验/NCT00281281
NCT00281281已完成4 期

Pharmacokinetics and Posology of Vancomycin in Adults Receiving ECMO

National Taiwan University Hospital2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2005年12月最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
24
试验地点
2
主要终点
pharmacokinetic parameters

研究概览

简要总结

  1. Vancomycin is a drug that requires precise dosing and close monitoring to avoid drug toxicity.

  2. There is limited data on the change of vancomycin pharmacokinetics in patients who need extracorporeal membrane oxygenation (ECMO).

  3. This control trial is to understand:

  4. whether the pharmacokinetics of vancomycin is influenced by the use ECMO

  5. design the most appropriate dose of vancomycin in adult patients using ECMO.

详细描述

  1. Vancomycin is a drug that requires precise dosing and close monitoring to avoid drug toxicity.

  2. Oftentimes it is used in intensive care units (ICU) for patients who need a life-saving machine for heart and lung failure called extracorporeal membrane oxygenation (ECMO).

  3. There is limited data on the change of vancomycin pharmacokinetics in these patients.

  4. This is a control trial using ICU patients who need vancomycin but not ECMO as a control to understand:

  5. whether the pharmacokinetics of vancomycin is influenced by the use ECMO

  6. design the most appropriate dose of vancomycin in adult patients using ECMO.

  7. After the 4th dose of vancomycin, blood was drawn at appropriate time spots (1 mL each) to determine the time concentration curve and to calculate the pharmacokinetic parameters for 2 groups of patients to determine if there is any difference.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • receiving ECMO for study group
  • without ECMO for control group (sex, age, creatinine clearance match with study group)

排除标准

  • severe burn (>30-40% BSA)
  • receiving continuous renal replacement therapy or hemodialysis concurrently

结局指标

主要结局

pharmacokinetic parameters

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

Loading locations...

相似试验

Pharmacokinetics of Vancomycin in Adults Receiving... | 临床试验