EUCTR2006-006334-18-BE进行中（未招募）不适用
Farmacokinetische evaluatie van de overschakeling van intraveneuze naar enterale toediening van moxifloxacine bij Intensieve Zorgen patiënten
niversity Hospital Gent0 个研究点开始时间: 2007年3月9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）
- 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 patiënten op antimicrobiële monotherapie met 400 mg mox IV (1 toediening per dag), die in aanmerking komen voor switch naar 400 mg mox enteraal (1 toediening per dag ).
- •- IV steady state bereikt: ten vroegste op 3e toediening
- •- Hemodynamisch stabiele patiënten
- •- Normale enterale voeding zonder prokinetica
- •- Aanwezigheid van een arteriële lijn of perifeer veneuze lijn
- •- Informed consent
- •- = of > 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
- •- Creatinineklaring < 30 ml/min/1.73 m²
- •- Transaminasen > 5x de bovengrens van normaal
- •- Vasopressoren
研究者
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