ISRCTN17027907已完成不适用
An assessment of the efficacy of oral chloroquine for the treatment of uncomplicated Plasmodium vivax malaria in Savannakhet Province, Lao People's Democratic Republic (PDR)
niversity of Oxford (UK)0 个研究点目标入组 100 人开始时间: 2008年1月23日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
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
- 性别
- All
入选标准
- •1. Written informed consent from patient or attending relative
- •2. Age greater than 1 year old, either sex
- •3. P. vivax infection (greater than 500 asexual stages/µL)
- •4. Acute uncomplicated malaria (World Health Organization [WHO] 2000)
- •5. Axillary temperature greater than 37.5°C
- •6. No full course of antimalarial treatment in the previous 3 days
- •7. High probability that patient will be able to complete 42 days follow up
排除标准
- •1. Inability or unwillingness to give informed consent
- •2. Mixed species malaria infections
- •3. Severe malaria (WHO, 2000)
- •4. History of allergy to chloroquine
- •5. Asymptomatic malaria
- •6. Low probability of 42 days follow up
研究者
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