EUCTR2008-003484-39-BE进行中（未招募）不适用
Farmacokinetische evaluatie van de eerste intraveneuze dosering van quinolones bij Intensieve Zorgen (IZ) patiënten met septische shock.
niversity Hospital Ghent0 个研究点开始时间: 2008年7月3日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •- IZ patiënt bij wie antimicrobiële intraveneuze therapie met 400 mg moxifloxacine (1 toediening per dag), of 500mg tavanic (2 toedieningen per dag), of ciproxine 400mg (3 toedieningen per dag) opgestart wordt.
- •- Eerste IV toediening
- •- Patiënt in acute fase van septische shock, met levophednood
- •- Aanwezigheid van een arteriële lijn
- •- Informed consent
- •- = 18 jaar
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- Dialysenood tijdens deelname aan de studie
研究者
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