ISRCTN80829842已完成不适用
Tribendimidine in the treatment of Clonorchis sinensis infection in the People?s Republic of China
Medical Research Council (UK)0 个研究点目标入组 75 人开始时间: 2012年3月20日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 75
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 (adults aged =18 years) infected with C. sinensis, as assessed by the presence of eggs in the stool
- •2. Signed written informed consent
- •3. Able and willing to be examined by a study physician at the beginning of the study and at the end-of study follow-up survey (3 - 4 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, psychiatric and neurological disorders as assessed by the medical doctor, upon initial clinical assessment
- •6. No known or reported hypersensitivity to tribendimidine or praziquantel
- •7. No known or reported history of chronical illness as cancer, diabetes, chronic heart, liver or renal disease
- •8. For females, not pregnant in the first trimester, as assessed by a female nurse (interview and pregnancy test if need be), upon initial clinical assessment
排除标准
- •1. For females, pregnancy in 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 hypersensitivity to tribendimidine or praziquantel
- •5. Known or reported psychiatric or neurological disorders
- •6. Use of any anthelmintic within the past month
- •7. Attending other clinical trials during the study
- •8. Absence of signed written informed consent sheet
研究者
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