EUCTR2013-003914-42-AT进行中（未招募）1 期
Multiple-dose Pharmacokinetics of Ceftaroline during continuous and intermittent renal replacement therapy in patients requiring renal replacement therapy - CEFTAROLINE_RRT
Medizinische Universität Wien, Univ.-Klinik für Innere Medizin I, Klinische Abteilung für Infetionen und Tropenmedizin0 个研究点目标入组 25 人开始时间: 2013年9月24日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 25
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
- •a)Age >18 years
- •b)Suspected or proven bacterial infection requiring parenteral antibiotic therapy.
- •c)Renal replacement therapy (continuous or intermittent)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •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 15
排除标准
- •a)Known hypersensitivity to ceftaroline or other cephalosporins, or severe hypersensitivity (anaphylactic reaction) to beta-lactam antibacterial agents.
- •b)An expected survival of less than two days.
- •c)Known pregnancy
- •d)Coadministration of valproic acid or probenecid, which cannot be discontinued for the duration of the study
- •e)Ceftarolin as monotherapy for resistent species or fungal infections.
- •f)Other reasons oposing the study participation on the discretion of the investigators
研究者
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