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临床试验/EUCTR2007-003223-20-BE
EUCTR2007-003223-20-BE进行中(未招募)不适用

Temocillin use in intensive care units:A Pharmacokinetic study of 6g per day in conventional administration vs. continuous infusion

Cliniques Universitaires St Luc - UC0 个研究点开始时间: 2007年7月6日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients will be eligible for participation in the study if they :
  • 1.are hospitalized in an intensive care unit
  • 2.have an abdominal or a pulmonary infection
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients will not be eligible to participate in the study if they:
  • 1.are confirmed or suspected infected by a bacteria non-susceptible to Temocillin
  • 2.are allergic to Temocillin or any other penicillin
  • 3.are pregnant women or lactating
  • 4.have participated in an investigational drug study within 4 weeks

研究者

发起方
Cliniques Universitaires St Luc - UC

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