跳至主要内容
临床试验/CTRI/2013/07/003850
CTRI/2013/07/003850已完成未知

A prospective pharmacokinetics and dose optimization study of extended infusion of Meropenem in adult critically ill cancer patientsâ??

Tata Memorial Hospital0 个研究点目标入组 25 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Inclusion criteria
  • Adult critically ill patients
  • Age 18 yr to 70 yrs
  • Known or suspected sepsis.
  • Baseline plasma creatinine concentration within upper limit of normal
  • Meropenem (MEROMER®) therapy initiated in ICU and expected to be continued for at least 3 days

排除标准

  • 未提供

研究者

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