ACTRN12613001003763已完成未知
A randomized control trial to evaluate the acceptability and accuracy of human papillomavirus (HPV) DNA self-sampling as a primary cervical screening test in women, compared with clinician-sampling.
Professor Eliza LY Wong, Associate Professor0 个研究点目标入组 390 人开始时间: 2013年9月10日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 390
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
- Randomised controlled trial
- 主要目的
- Diagnosis
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 35 Years 至 65 Years（—）
- 性别
- Female
入选标准
- •Female aged 35 to 65 who have ever had sexual experience and are able to give a written informed consent.
排除标准
- •Women who have never had sex, had total hysterectomy, or currently pregnant were excluded from the study.
研究者
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