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临床试验/TCTR20210617001
TCTR20210617001招募中4 期

Effect of vancomycin loading dose on AUC0-24 target attainment in pediatric sepsis patients

Kritsaporn Sujjavorakul0 个研究点目标入组 78 人开始时间: 2021年6月17日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
78

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
3 Months 至 18 Years(—)
性别
All

入选标准

  • 1. Age 3 months to 18 years at the day of the first dose vancomycin
  • 2. Pediatric sepsis patients
  • 3. Informed consent by one parent or the legal guardian

排除标准

  • 1. Receiving extracorporeal organ support including hemodialysis, peritoneal dialysis (PD), continuous renal replacement therapy (CRRT), plasmapheresis, blood purification, artificial liver support systems, and extracorporeal membrane oxygenation (ECMO)
  • 2. Previous vancomycin treatment within 1 weeks prior to the day of study in subject with normal kidney function at baseline or within 4 weeks prior to the day of study in subject with renal impairment.

研究者

发起方
Kritsaporn Sujjavorakul

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