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临床试验/PACTR202001919442161
PACTR202001919442161已完成3 期

Efficacy and safety of Praziquantel alone or in combination with Artemisinin-based combinations in the treatment of children with Schistosoma mansoni in Mwea, Kirinyaga County, Kenya

Kenya Medical Research Institute0 个研究点目标入组 540 人开始时间: 2019年12月7日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
540

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
13 Year(s) 至 18 Year(s)(—)
性别
All

入选标准

  • For participants to be enrolled in the study they have to meet ALL of the following criteria:
  • Aged between 6 and 15 years old (confirmed from the date of birth recorded on the school registers),
  • Testing positive for S. mansoni infection (confirmed by presence of eggs in stool).
  • Residing in Mwea East and Mwea West, Kirinyaga County
  • Able to take oral treatment
  • Respective parent/ guardian provides written informed consent for the child to participate in the study
  • Child provides written assent to participate in the study

排除标准

  • Potential participants will be excluded for any of the following reasons:
  • Weighing more than 50 kg,
  • Haemoglobin level = 5.0g/dL
  • Signs of severe malnutrition (defined as severe wasting or MUAC <12cm)
  • Hypersensitivity to Artesunates, sulfonamides or praziquantel.
  • Use of an anti-malaria or anti-schistosomial drug within 28 days before enrollment in the study.

研究者

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