ACTRN12622000272796撤回4 期
Evaluation of the safety, tolerability and effectiveness of weekly tafenoquine for malaria prophylaxis in Vietnam People’s Army personnel in South Sudan
Australian Defence Force Malaria and Infectious Disease Institute0 个研究点目标入组 63 人开始时间: 2022年2月14日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 撤回
- 发起方
- 入组人数
- 63
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1)Adults (male and female).
- •2)Glucose-6-phospate dehydrogenase (G6PD) normal enzyme activity levels (>70%) of the site median value for G6PD normals using a quantitative G6PD test.
- •3)Willing and able to comply with all monitoring visits, physical examination, adverse events questionnaire, laboratory tests, and other study procedures.
- •4)Willingness to complete an acceptability questionnaire.
- •5)Completion of the written informed consent process prior to undertaking any study-related procedure.
排除标准
- •1)G6PD deficiency.
- •2)Prior or current history of nervous system and psychiatric disorders.
- •3)Any participant who is directly involved in conducting the study.
- •4)Any participant with poor peripheral venous access for blood sampling.
- •5)Known hypersensitivity reactions to primaquine.
- •6) Pregnant women.
研究者
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