jRCTs031240746招募中不适用
A Randomized Clinical Trial to Compare the Efficacy and Immunogenicity of Single-Dose versus Two-Dose HPV Vaccination in Men (HPV-ONE)
未提供0 个研究点目标入组 220 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 220
- 主要终点
- -
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
- Randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Prevention Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 18age old over 至 No limit（—）
- 性别
- Male
入选标准
- •Male individuals aged 18 years or older at the time of consent.
- •Individuals who have provided written informed consent to participate in the study.
排除标准
- •Individuals with known allergies to the treatment medication.
- •Individuals who regularly use steroids or immunosuppressive agents.
- •Individuals with a history of receiving the 2-valent, 4-valent, or 9-valent HPV vaccine.
- •Individuals deemed unsuitable for study participation by the attending physician.
结局指标
主要结局
-
HPV16 IgG seropositivity rate at Week 96
次要结局
- New persistent infection in the pharynx or anus(Week 48 and Week 96)
- New cytological abnormalities(Week 48 and Week 96)
- Histological abnormalities(Week 48 and Week 96)
研究者
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