JPRN-UMIN000010843已完成未知
Randomized controlled trial to evaluate the efficacy of concurrent liquid-based cytology (LBC) and HPV DNA testing versus LBC alone for the primary cervical cancer screening - Cervical cancer screening trial by randomization of HPV testing intervention for upcoming screening (CITRUS study)
The Japanese Society of Clinical Cytology0 个研究点目标入组 30,000 人开始时间: 2013年6月1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
- 30,000
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
- 30years-old 至 65years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •1) Women who will receive planed HPV DNA testing by local governmental cervical cancer program next six years. 2) Women who have had cervical invasive cancer before. 3) Women who have underwent cervical conization. 4) Women who have underwent hysterectomy. 5) Women who have had or have the cytological abnormalities and are under follow-up. 6) Pregnant women. 7) Women judged ineligible for this trial by physician.
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