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临床试验/NCT04203784
NCT04203784已完成不适用

Meropenem and Piperacillin Plasma Concentrations During CRRT

Karolinska University Hospital1 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2012年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
135
试验地点
1
主要终点
Plasma antibiotic concentrations at mid and end of dosing interval

研究概览

简要总结

This observational study reports meropenem and piperacillin plasma concentrations in patients treated with either antibiotic and simultaneous continuous renal replacement therapy (CRRT).

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients treated in the study ICU and
  • simultaneous CRRT and antibiotic treatment with either meropenem or piperacillin-tazobactam.

排除标准

  • 未提供

结局指标

主要结局

Plasma antibiotic concentrations at mid and end of dosing interval

时间窗: 1 week

The percentage of patients having a concentration above the highest MIC (minimal inhibitory concentration) breakpoint for pathogens considered susceptible for the antibiotic.

Relationships between plasma antibiotic concentrations and CRRT dose.

时间窗: 1 week

We will report the correlation between measured plasma concentrations of either antibiotic and the intensity of the CRRT treatment.

Influence of residual diuresis on the measured plasma antibiotic concentrations.

时间窗: 1 week

We will report the correlation between measured plasma concentrations of either antibiotic and residual diuresis.

次要结局

未报告次要终点

研究者

发起方
Karolinska University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Johan Petersson

Senior ICU Consultant

Karolinska University Hospital

研究点 (1)

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