PACTR2010020001862624尚未招募未知
Comparison of the safety, efficacy and tolerability of artemether¬-lumefantrine and artesunate amodiaquine in Nigerian pregnant women with acute uncomplicated falciparum malaria
Marcel Ukah0 个研究点目标入组 0 人开始时间: 2010年1月21日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
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
- 年龄范围
- 18 Year(s) 至 55 Year(s)（—）
- 性别
- Female
入选标准
- •a)Microscopically-confirmed P. falciparum malaria with parasitaemia of atleast one plus(1-10 parasites /100 thick film field).
- •b)Fever (T of 37.50C) or a history of fever,headaches,body pains within 24 hours of presentation
- •c)Ability to give informed consent
- •d)Willingness/ability to comply with follow up visits.
排除标准
- •a)Severe malaria or danger signs of severe malaria (e.g. loss of consciousness, convulsions, anuria)
- •b)Women in the first 13 weeks of pregnancy i.e. 1st trimester
- •c)Use of any anti-malarial drug other than sulphadoxine pyrimethamine less than 7 days before presentation
- •d)Other chronic illness e.g. hypertension, sickle cell.
- •e)Other pregnancy related diseases e.g. eclampsia, antepartum hemorrhage
- •f)History of reaction to any of the study drugs
- •g)Patients not tolerating orally.
研究者
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