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临床试验/2024-518857-41-00
2024-518857-41-00
尚未招募
4 期

Concomitant HPV vaccination and HPV screening for rapid elimination of HPV infection and cervical cancer in Sweden

Region Stockholm21 个研究点 分布在 1 个国家目标入组 150,000 人开始时间: 2024年11月29日最近更新:

概览

阶段
4 期
状态
尚未招募
入组人数
150,000
试验地点
21
主要终点
Uptake of HPV vaccine in eligible women, by county and age strata.

概览

简要总结

The study aims to evaluate whether organised, concomitant HPV vaccination and HPV screening offered by the Swedish cervical screening program to all resident women aged 23-25 will result in a more rapid elimination of HPV infection in Sweden. This objective will be examined at the population level.

入排标准

年龄范围
18 years 至 64 years(18-64 Years)
性别
Female
接受健康志愿者

入选标准

  • Eligible women will include resident women within the age range of 23- 25 due for invitation to organised cervical cancer screening who consent to participate in the study.

排除标准

  • Known history of severe allergic reaction or hypersensitivty to any of the components of the HPV vaccine. For GARDASIL 9: Amorphous aluminium hydroxyphosphate sulphate adjuvant, Sodium chloride, L-histidine, Polysorbate 80 or Sodium borate.
  • Known history of immune-related disorders.
  • Current acute severe febrile illness, except for minor infections such as a cold, mild upper respiratory infection or low-grade fever.
  • Administration of immunoglobulin or blood-derived products within 6 months prior to scheduled HPV vaccine first dose.
  • Current pregnancy (reported).
  • Hysterectomized women.

结局指标

主要结局

Uptake of HPV vaccine in eligible women, by county and age strata.

Uptake of HPV vaccine in eligible women, by county and age strata.

次要结局

  • Compliance with HPV vaccine administration Schedule.

研究者

申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Joakim Dillner

Scientific

Region Stockholm

研究点 (21)

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