EUCTR2010-019955-23-GB进行中(未招募)不适用
To evaluate the pharmakcokinetics, tolerability and short term safety of ciprofloxacin in neonates and infants with suspected (or proven) Gram Negative Infection Open Label pilot PK study - TINN Treat Infections in Neonates Program(TINN-PK) - TINN Treat Infections in Neonates Pharmocokinetics of Ciprofloxacin
iverpool Women's NHS Foundation Trust0 个研究点开始时间: 2010年11月26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
- •Neonates and infants 24 - 52 weeks gestation who are receiving ciprofloxacin following a clinical decision by their attending physician to treat suspected or proven sepsis.
- •Parental consent to participate
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years)
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years)
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Likely not to survive for more than 48 hours in judgement of attending physician.
- •Significant liver or renal impairment.
研究者
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