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
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