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临床试验/TCTR20150623001
TCTR20150623001已完成4 期

Evaluating the efficacy of artesunate-mefloquine on the Thai-Myanmar border and the relative roles of resistance genetic markers: A retrospective cohort study

ot available0 个研究点目标入组 1,022 人开始时间: 2015年6月23日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
1,022

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
0 Years 至 99 Years(—)
性别
All

入选标准

  • •Non pregnant patients of any age and sex who received treatment for uncomplicated malaria between January 2003 to December 2013
  • •Symptomatic of malaria infection, i.e. history of fever or tympanic temperature ≥37.5°c
  • •Microscopically confirmed asexual stages of P. falciparum ≥ 5/500 WBC (alone or mixed with non- P. falciparum species)
  • •Received fully supervised treatment of mefloquine-artesunate

排除标准

  • •Pregnant woman
  • •P. falciparum asexual stage parasitaemia greater than or equal to 4% red blood cells (175 000/µL).
  • •Signs or symptoms indicative of severe malaria:
  • •Mefloquine treatment within 60 days of current episode of malaria
  • •Splenectomy

研究者

发起方
ot available

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Monitoring the efficacy of mefloquine-artesunate... | 临床试验