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临床试验/EUCTR2010-021050-20-BE
EUCTR2010-021050-20-BE进行中(未招募)1 期

Assessment of the optimal dosing of piperacillin-tazobactam in intensive care unit patients: extended versus continuous infusion

Ghent University Hospital0 个研究点目标入组 30 人开始时间: 2010年7月20日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
30

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

  • o Adult patients (> 18 years) admitted on the intensive care unit (surgical and medical surgery).
  • o Starting a treatment with piperacilline/tazobactam
  • o Signed informed consent
  • o Hematocriet >= 21%
  • o Available arterial line
  • 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

  • o age <18 or >75 years
  • o patient's weight <50 or >100 kg
  • o renal insufficiency (estimated clearance < 50 ML /MIN)
  • o haemodialysis
  • o WBC < 1000 103 µl
  • o estimated survival <5 days
  • o meningitis or other proven infections of the CNS
  • o IgE-mediated allergy to penicillins
  • o pregnancy
  • o patients having participated in another study <30 days before
  • o retrospectively, marked deterioration of the renal function during the study period
  • o retrospectively, treatment < 96 h

研究者

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