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临床试验/EUCTR2012-000904-14-AT
EUCTR2012-000904-14-AT进行中(未招募)不适用

PHARMACOKINETICS OF MICAFUNGIN DURING CONTINUOUS VENOVENOUS HEMOFILTRATION - MICA_HDF

Medizinische Universität Wien0 个研究点目标入组 10 人开始时间: 2012年3月29日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Age 19 to 70 years
  • Suspected or proven candia infection requiring parenteral antifungal therapy
  • Continuous venovenous hemofiltration because of an acute renal failure
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 6
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 4

排除标准

  • Known history of hypersensitivity to echinocandins.
  • An expected survival of less than three days.
  • Known alcohol dependency, epilepsy, pregnancy or liver failure.
  • Sooroesophagitis

研究者

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