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临床试验/TCTR20190515001
TCTR20190515001招募中4 期

Pharmacokinetic study and safety of levofloxacin in pediatric tuberculosis treatment

Center of Excellence for Pediatric Infectious Diseases and Vaccines0 个研究点目标入组 20 人开始时间: 2019年5月15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
20

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 15 Years(—)
性别
All

入选标准

  • 1) age 3 months to 15 years
  • 2) having an indication to used levofloxacin for tuberculosis treatment (MDR-TB, Hr-TB, toxicity from the first line drug)
  • 3) weight 6-40 kilogram
  • 4) primary caregiver give consent and children aged more than 7 years give assent.

排除标准

  • 1) History allergic to levofloxacin
  • 2) Levofloxacin resistant tuberculosis
  • 3) Medical history of QT prolong
  • 4) Pregnancy

研究者

发起方
Center of Excellence for Pediatric Infectious Diseases and Vaccines

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Pharmacokinetic study and safety of levofloxacin in... | 临床试验