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临床试验/ISRCTN90823663
ISRCTN90823663已完成未知

Efficacy and tolerability of artemether lumefantrine and amodiaquine artesunate for the treatment of uncomplicated falciparum malaria in Burkina Faso

ational Malaria Control Program (Burkina Faso)0 个研究点目标入组 780 人开始时间: 2012年1月30日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
780

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. Age > 6 months
  • 2. Weight > 5 kg
  • 3. Fever (> 37.5ºC axillary) or history of fever in the previous 24 hours
  • 4. Absence of any history of serious side effects to study medications
  • 5. No evidence of a concomitant febrile illness
  • 6. Provision of informed consent and agreement to follow-up for 28 days
  • 7. No evidence of severe malaria or danger signs
  • 8. Absence of repeated vomiting of study medications on day 0
  • 9. P. falciparum mono-infection
  • 10. Parasite density > 2000/ul and < 200,000/ul

排除标准

  • 1. Severe malaria
  • 2. Unable to respect the follow-up schedule
  • 3. Known allergy to the study medication
  • 4. Other chronic disease requiring care

研究者

发起方
ational Malaria Control Program (Burkina Faso)

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