IRCT2016101730345N1已完成早期 1 期
Pharmacokinetics and safety of high-dose intravenous daptomycin in infected hemodialysis patients
适应症
试验速览
- 阶段
- 早期 1 期
- 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 years 至 no limit（—）
- 性别
- All
入选标准
- •Inclusion: patients > 18 years, requiring conventional hemodialysis for chronic renal failure hospitalized at the University Hospital of Poitiers (CHU de Poitiers) and presenting a CRBSI.
- •Exclusion: pregnant or breeding women, pneumonia, septic shock (which may affect pharmacokinetic parameters and therefore not represent the principal hemodialysis population); CPK >3ULN; known hypersensitivity to Daptomycin.
排除标准
- 未提供
研究者
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