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临床试验/NCT00460369
NCT00460369已完成不适用

Sulfadoxine-Pyrimethamine Versus Artemether-Lumefantrine Versus Amodiaquine-Artesunate Coformulation in Uncomplicated Plasmodium Falciparum Malaria : an Open Randomized Study

Institut de Recherche pour le Developpement1 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2007年4月最近更新:
适应症
干预措施
相关药物

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

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

Active Comparator

sulfadoxine-pyrimethamine

干预措施: sulfadoxine-pyrimethamine (Drug)

2

Active Comparator

artemether-lumefantrine

干预措施: artemether-lumefantrine (Drug)

3

Active Comparator

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)

研究者

申办方类型
Other Gov

研究点 (1)

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