EUCTR2014-003177-42-DK进行中（未招募）1 期
Multinational study assessing the acceptability and determinants of compliance to HPV vaccination to women in screening ages 30 to 45 years
Catalan Institute of Oncology0 个研究点目标入组 3,250 人开始时间: 2014年10月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 3,250
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •Adult women aged 30-45 years attending routine cervical cancer screening with no previous history of HPV vaccine administration
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 3250
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- Women with a known history of severe allergic reaction or hypersensitivity to any of the components of the vaccine.
- •- Women with a known history of immune-related disorders.
- •- Women with current acute severe febrile illness, except for minor infections such as a cold, mild upper respiratory infection or low-grade fever. When recovered, the vaccine can be administered.
- •- Pregnant women, women planning to get pregnant in the coming 12 months, and women who are breastfeeding
- •- Hysterectomized women
- •- Administration of immunoglobulin or blood-derived products within 6 months prior to the first HPV dose
研究者
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