ISRCTN79195095已完成不适用
Efficacy and safety of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in Eritrea
World Health Organization (WHO) (Switzerland)0 个研究点目标入组 180 人开始时间: 2007年9月7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
- 180
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. All ages, 6 months and above
- •2. Single infection with P. falciparum
- •3. Parasitaemia of 1,000 - 100, 000 asexual forms per µl
- •4. Axillary temperature of 37.5°C or oral/rectal temperature of 38°C, or history of fever in the previous 24 hours
- •5. Ability to swallow oral medication
- •6. Ability and willingness to comply with the study protocol for the duration of the study and to comply with the study visit schedule
- •7. Informed consent from the patient or from a parent or guardian in case of children
排除标准
- •1. Presence of general danger signs among children less than 5 years old or other signs of severe and complicated falciparum malaria according to current WHO definitions
- •2. Mixed or mono-infection with another Plasmodium species
- •3. Presence of severe malnutrition defined as a child whose weight-for-height is below 3 Standard Deviation (SD)
- •4. Presence of febrile conditions due to diseases other than malaria (measles, acute lower tract respiratory infection, severe diarrhoea with dehydration, etc.), or other known underlying chronic or severe diseases (e.g. cardiac, renal, hepatic diseases, Human Immunodeficiency Virus [HIV]/Acquired Immune Deficiency Syndrome [AIDS])
- •5. History of hypersensitivity reactions to any of the drug(s) being tested or used as alternative treatment
- •6. Pregnancy or positive pregnancy test or lactating
研究者
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