CTIS2023-506792-94-00进行中（未招募）1 期
VulVaccin study: Adjuvant nonavalent HPV vaccination in women treated for vulvar HSIL, a Randomised Placebo Controlled Trial.
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 498
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
- 18 至 65+（—）
入选标准
- •Women 18 years or older, Vulvar High-grade Squamous Intraepithelial Lesion (HSIL), histologically proven, Planned for treatment (surgical, laser or imiquimod) for vulvar High Grade Squamous Intraepithelial Lesion
排除标准
- •Prior HPV vaccination, (Micro-) invasive carcinoma or history of HPV related genital carcinoma (cervix, anal, vulva), Pregnancy, Women allergic to vaccine components, HIV infection, Immune compromised patients (currently on immunosuppressive medication)
研究者
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