跳至主要内容
临床试验/NCT03720132
NCT03720132终止不适用

Optimization of Therapeutic Drug Monitoring of Vancomycin in Pediatric Patients With an Implanted Port Catheter

Universitaire Ziekenhuizen KU Leuven2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2014年6月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
10
试验地点
2
主要终点
Vancomycin trough levels via port catheter and peripheral vein

研究概览

简要总结

The goal of this study is to verify whether extensive flushing of the port catheter in patients with catheter related blood stream infection will lead to correct vancomycin trough levels, taken via the port catheter and compared with simultaneously taken peripheral samples.

详细描述

In this study, extensive flushing of the port catheter prior to blood sampling to determine vancomycin trough levels, will be compared with normal flushing. To ascertain correctness of the trough levels taken via the central catheter, sampling will occur through a peripheral catheter simultaneously.

Flushing will be done with sodium chloride 0.9 % solution.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Pediatric patients with a port catheter
  • Treated with systemic vancomycin and/or vancomycin "lock"

排除标准

  • Age > 18 years
  • Active downgrading of care

结局指标

主要结局

Vancomycin trough levels via port catheter and peripheral vein

时间窗: At steady state i.e. approximately 36 hours after initation of the treatment or a change in dose

Vancomycin trough levels will be determined, both on peripheral blood and blood taken via the port catheter and will be compared.

次要结局

未报告次要终点

研究者

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

Isabelle Spriet

PharmD, PhD

Universitaire Ziekenhuizen KU Leuven

研究点 (2)

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