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临床试验/NL-OMON38737
NL-OMON38737已完成不适用

Pharmacokinetics of nasally administered tobramycin and colistin in Cystic Fibrosis - SPOEL study

HagaZiekenhuis0 个研究点目标入组 10 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Confirmed diagnose of Cystic Fibrosis based on genotyping or a positive sweat test
  • 2. Age >= 18 years
  • 3. Intravenous course of tobramycin in the past, but within the age of >= 18 years, with a creatinine value measured during that same intravenous course of tobramycin

排除标准

  • 1. Kidney dysfunction (defined as estimated Glomerular Filtration Rate of < 50 ml/min)
  • 2. Liver dysfunction (defined as at least one of the liver enzymes >= 3 times the normal value)
  • 3. Intravenous treatment with aminoglycosides or polymyxins <= 48 hours
  • 4. Acute pulmonary exacerbation (defined by Fuchs criteria)
  • 5. Allergy or intolerance for aminoglycosides or polymyxins
  • 6. Recent surgery of ear, nose or sinuses (< 3 months before study entry)

研究者

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