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临床试验/ISRCTN23425032
ISRCTN23425032已完成不适用

Mefloquine, artesunate, mefloquine-artesunate and tribendimidine in the treatment of Opisthorchis viverrini infection in Laos

Swiss Tropical and Public Health Insitute (Switzerland)0 个研究点目标入组 100 人开始时间: 2010年3月16日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100

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. Patients (male and female schoolchildren older than 8 years) infected with O. viverrini, as assessed by the presence of eggs in the stool
  • 2. Weight of patient greater than 25 kg
  • 3. Able and willing to be examined by a study physician at the beginning of the study and at the end-of study (3 weeks post-treatment)
  • 4. Able and willing to provide multiple stool samples at the beginning and end of study
  • 5. Absence of major systemic illnesses, as assessed by the medical doctor, upon initial clinical assessment
  • 6. Absence of psychiatric and neurological disorders
  • 7. No known or reported hypersensitivity to mefloquine, tribendimidine and/or artesunate
  • 8. No known or reported history of chronic illness as cancer, diabetes, chronic heart, liver or renal disease
  • 9. Signed written informed consent sheet
  • 10. For females aged 12 years and above, not pregnant in the first trimester, as assessed by a pregnancy test, upon initial clinical assessment

排除标准

  • 1. Pregnancy first trimester
  • 2. Presence of any abnormal medical condition, judged by the study physician
  • 3. History of acute or severe chronic disease
  • 4. Known or reported psychiatric or neurological disorders
  • 5. Use of artesunate, artemether, any ACT, mefloquine or praziquantel within the past month
  • 6. Attending other clinical trials during the study

研究者

发起方
Swiss Tropical and Public Health Insitute (Switzerland)

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