跳至主要内容
临床试验/NCT05221216
NCT05221216已完成不适用

Single-center Retrospective Observational Study of Cotrimoxazole Dosing in Intensive Care Unit

Centre Hospitalier Universitaire de Saint Etienne1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2021年10月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
5
试验地点
1
主要终点
plasma concentrations of cotrimoxazole (mg/l)

研究概览

简要总结

Trimethoprim/sulfamethoxazole (TMP/SMX, cotrimoxazole) is the first-line therapy for Pneumocystis jirovecii pneumonia and bacterial infections in critically ill patients, where acute kidney injury (AKI) and renal replacement therapy (RRT) are regularly observed. Both may change half-life and subsequent concentrations. Specifically, Trimethoprim (TMP) is eliminated renally, whereas sulfamethoxazole (SMX) elimination is 80%metabolic/20%renal. Despite decades of cotrimoxazole use, data in acute kidney injury (AKI) are scarce and no consensus on dosing strategy has been established. Besides, pharmacodynamic parameter has not been determined, leading to an uncertainty on the dosing regimen.

详细描述

The objective is to compare the plasma concentrations of patients with acute renal failure (ARF) or requiring extra renal replacement therapy (RRT) with those of patients without these characteristics to look for differences in concentration.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

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

  • Patient hospitalized in Intensive Care Units between October 2020 and July 2021 with infection treated with cotrimoxazole

排除标准

  • 未提供

结局指标

主要结局

plasma concentrations of cotrimoxazole (mg/l)

时间窗: From the antibiotic initiation until the patient is discharged from the ICU with a maximal time frame of 10 weeks

pharmacokinetic cotrimoxazole

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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