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临床试验/PACTR201612001901313
PACTR201612001901313已完成未知

Effectiveness of the combination of dihydroartemisinin and piperaquine for prevention of falciparum malaria during pregnancy in Tanzania

MUHAS0 个研究点目标入组 1,000 人开始时间: 2016年12月2日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
MUHAS
入组人数
1,000

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 35 Year(s)(—)
性别
Female

入选标准

  • i.Viable pregnancy assessed by UPT
  • ii.Gestational age 16 to 32 weeks (inclusive) determined by fundal height
  • iii. No prior history of IPTp use for current pregnancy
  • iv.Willing to participate and complete the study schedule
  • v.Willing to sign or thumb print informed consent
  • vi. Resident of study area and intending to stay in the area for the duration of the follow-up
  • vii.Willing to deliver at the health facility

排除标准

  • i.Residence outside study area or planning to move out in the 12 months following enrolment
  • ii.High risk pregnancy, including any pre-existing illness likely to cause complication of pregnancy (hypertension, diabetes, asthma, epilepsy, renal disease, liver disease, fistula repair, leg or spine deformity)
  • iii.Severe anemia requiring blood transfusion (Hb ¿ 7.0 g/dL) at enrolment
  • iv.Known allergy or previous adverse reaction to any of the study drugs
  • v.Unable to give informed consent (for example due to mental disability)
  • vi.Previous inclusion in the same study

研究者

发起方
MUHAS

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