Sulfadoxine-Pyrimethamine Versus Artemether-Lumefantrine Versus Amodiaquine-Artesunate Coformulation in Uncomplicated Plasmodium Falciparum Malaria : an Open Randomized Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 240
- 试验地点
- 1
- 主要终点
- efficacy
研究概览
简要总结
Malaria is a life-threatening disease especially in small children. A high degree of Plasmodium falciparum resistance to chloroquine has already spread to South-Benin where this study is taking place. In the past few years, the recommendation for a first-line treatment in this area has moved from chloroquine to sulfadoxine-pyrimethamine (SP). There is growing evidence that Plasmodium falciparum resistance to SP has come to South-Benin. The aim of the study is to compare the efficacy of SP to two compact artemisinin-based therapies (ACT): artemether-lumefantrine and the amodiaquine-artesunate coformulation. ACT will be unsupervised.
The primary endpoint is an effectiveness comparison (PCR corrected) at day 28. Secondary outcomes are effectiveness comparisons (PCR corrected) at day 14 and 42 and a study on the relationships between ACT PK data (day 3) and outcome.
Expected total enrollment: 225 patients
Study start: April 2007; expected completion: December 2007
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 6 Months 至 119 Months(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •6-119 months old
- •fever or history of fever of less than 24 hours
- •p falciparum parasitemia > 1000 trophozoïtes/µL
- •informed consent signed
排除标准
- •danger or severity signs of malaria
- •known underlying chronic disease
- •Hb < 5g/dL
- •adequate malaria treatment taken within 3 days before visit
研究组 & 干预措施
1
sulfadoxine-pyrimethamine
干预措施: sulfadoxine-pyrimethamine (Drug)
2
artemether-lumefantrine
干预措施: artemether-lumefantrine (Drug)
3
amodiaquine-artesunate coformulation
干预措施: amodiaquine-artesunate coformulation (Drug)
结局指标
主要结局
efficacy
时间窗: day 28
次要结局
- effectiveness comparisons (PCR corrected)(day 14 and day 42)
- incidence of adverse events(day 42)
