EUCTR2015-004251-47-BE进行中（未招募）1 期
Validation of central venous (Port A Cath®) blood draws for ciprofloxacin pharmacokinetic research in patients under treatment for childhood cancer. - Cipro-onco-validation
Z Brussel0 个研究点目标入组 15 人开始时间: 2015年10月12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
- 15
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
- •Children who
- •are between 1 month and 18 years of age
- •are under treatment for any type of childhood cancer
- •use ciprofloxacin intravenous for selective bowel decontamination as part of regular treatment
- •have a PAC (port a cath) for intravenous medication and blood draws.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 15
- •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) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Children will be excluded from this study if we are unable to
- •obtain informed consent of both parents and assent of the child (if he/she is over 12 years of age)
- •aspire blood from the PAC (port a cath).
研究者
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Unknown
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