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临床试验/NCT01894347
NCT01894347已完成不适用

Prospective Observational Pilot-study for the Evaluation of the Nephro- an Neurotoxicity in the Anti-infectious Therapy With Inhalative Colistin Therapy for Patients With Ventilator-associated Pneumonia (VAP)

Charite University, Berlin, Germany1 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2013年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
9
试验地点
1
主要终点
Number and frequency of adverse events (nephro- or neurotoxicity after aerosolised colistin therapy)

研究概览

简要总结

Multi-Drug resistant pathogens (MDR) are reported worldwide with increasing incidence, especially in intensive care settings.

One of the drugs which are effective against MDRs, is colistin (polymyxin E). This agent has been reintroduced in response to the increase of MDR pathogens and might be used more often in the future. Data on safety regarding the most important side effects are not sufficiently available. l This study evaluates the toxicity in patients who receive aerosolized colistin.

详细描述

There is growing evidence that patients in the ICU setting have a special risk profile for consecutive colonization and possible infection due to MDR pathogens.

One therapy option is the use of inhalative colistin, as this agent has been demonstrated to be effective against these pathogens. Data on pharmacodynamics or - kinetics are transferred from older studies or from other patient populations. For patients with pulmonary colonization or infection due to an MDR pathogen the systemic resorption of the drug is not known, consequently systemic side effects including kidney or neural damage are not predictable.

This study focus on patients with inhalative colistin therapy and uses therapeutic drug monitoring to determine the rate of systemic resorption of colistin. For the evaluation of neurotoxicity function of peripheral nerves (neve conduction velocity) and of the eighth cranial nerve is monitored. Nephrotoxicity is estimated by creatinine level (-clearance) and the RIFLE criteria.

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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Number and frequency of adverse events (nephro- or neurotoxicity after aerosolised colistin therapy)

时间窗: 28 days

Adverse events are measured based on validated criteria: 1. creatinine-clearance and RIFLE-criteria 2. Neuromonitoring (nerve conduction velocity, EEG)

次要结局

  • Serum levels of colistin and β-Lactam antibiotics (e.g. Meropenem)in mg/L(3 days)
  • Serum concentration of colistin and β-Lactam antibiotics(3 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Maria Deja

Prof. Dr. med. Maria Deja

Charite University, Berlin, Germany

研究点 (1)

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