EUCTR2005-004455-35-AT进行中（未招募）不适用
Plasma and abscess fluid pharmacokinetics of cefpirome and moxifloxacin after single dose and multiple dose administration - Abscess-Cef-Moxi
Department of Clinical Pharmacology, Medical University of Vienna0 个研究点目标入组 20 人开始时间: 2005年10月18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
- 入组人数
- 20
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
- •Female or male, aged between 18 and 90 years.
- •Written informed consent.
- •Abscess formation or abdominal cyst scheduled to drainage.
- •Plasma creatinine <1.5 mg/dL
- •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
- •Pregnancy or lactation.
- •Hemodialysis or hemofiltration
- •Allergy or hypersensitivity against study drugs
- •Massive edemata or hypernatremia
- •Reduced liver function (Child-Pugh A, B, C)
- •Relevant prolongation of QT-interval
- •CNS-diseases which predispose for cramps
研究者
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