PACTR202001893991170已完成2 期
Mosquitocidal effect and pharmacokinetics of different ivermectin dose regimens in preparation for BOHEMIA cluster randomized controlled trial.
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 36
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- All
入选标准
- •i.Male or female 18 - 45 years old;
- •ii.Body weight over 50Kg;
- •iii.Good health or no medical conditions that could interfere with the study according to the opinion of the study clinician;
- •iv.Willingness to participate voluntarily in all study procedures;
- •v.Plans to remain available for study participation within the next 7 months;
- •vi.Use of effective method of contraception documented through a family planning card for the duration of study for female participants;
- •vii. Ability to give informed consent and communicate with the study personnel.
排除标准
- •i.Feeling sick or presenting signs of sickness, which are considered by the project physician to not be temporary condition or likely to resolve before pre-enrolment screening;
- •ii.Body weight below 50Kg;
- •iii.Positive for malaria rapid diagnostic test (mRDT);
- •iv.Lactating or pregnant verified through ß-hCG urine test;
- •v.Clinically significant laboratory abnormality as judged by the study clinician;
- •vi.Receiving or having received in the past 30 days treatments that could, in the eyes of the investigator, interfere with the study;
- •vii.Hypersensitivity against any of the study drugs.
研究者
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