NCT01506128已完成不适用
Exploration of Optimal Experimental Settings to Detect Human Papillomavirus From Menstrual Blood in Women With High-grade Squamous Intraepithelial Lesion or High-risk Human Papillomavirus Infection
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 19
- 试验地点
- 1
- 主要终点
- HPV detection rate in menstrual blood
研究概览
简要总结
The investigators tried to know whether a virus causing cervical cancer could be detected in menstrual blood and to set up a experimental setting to detect the virus.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Premenopausal women with HSIL at Pap test or high-risk HPV
排除标准
- •Suspicious cancer
结局指标
主要结局
HPV detection rate in menstrual blood
时间窗: First period after enrollment usually within 2 months after enrollment
The first menstrual period after enrollment is assumed to occur within 2 months. At that time, the participant used pads and send the used pads to investigators. The investigator do procedures to detect HPV in pads.
次要结局
未报告次要终点
研究者
Kidong Kim
Assistant Professor, Department of Obstetrics and Gynecology
Seoul National University Bundang Hospital
研究点 (1)
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