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临床试验/EUCTR2010-019955-23-GB
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

发起方
iverpool Women's NHS Foundation Trust

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