PACTR2010020001429343Other未知
EVALUATION OF THE SAFETY AND EFFICACY OF MEFLOQUINE AS INTERMITTENT PREVENTIVE TREATMENT FOR MALARIA IN PREGNANCY
FCRB0 个研究点目标入组 0 人开始时间: 2009年5月27日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- Other
- 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
- 15 Year(s) 至 50 Year(s)（—）
- 性别
- Female
入选标准
- •Permanent resident in the area
- •Gestational age at the first antenatal visit < 28 weeks
- •Signed informed consent
- •Agreement to deliver in the study site's maternity wards
排除标准
- •Residence outside the study area or planning to move out in the following 18 months from enrollment
- •Gestational age at the first antenatal visit > 28 weeks of pregnancy
- •Known history of allergy to sulfa drugs or mefloquine
- •Known history of severe renal, hepatic, psychiatric or neurological disease
- •MQ or halofantrine treatment in the preceding 4 weeks
- •HIV infection
- •Participating in other studies
研究者
相似试验
Unknown
不适用
EVALUATION OF THE SAFETY AND EFFICACY OF MEFLOQUINE AS INTERMITTENT PREVENTIVE TREATMENT FOR MALARIA IN PREGNANCY IN HIV+ PATIENTSHIV/AIDSPregnancy and ChildbirthMalariaPACTR2010020001813440FCRB
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