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临床试验/NCT03747770
NCT03747770Unknown不适用

A Community Intervention Effectiveness Study: Single Dose or Two Doses of Bivalent HPV Vaccine (CERVARIX) in Female School Students in Thailand

International Vaccine Institute2 个研究点 分布在 1 个国家目标入组 18,000 人开始时间: 2018年12月17日最近更新:
适应症

试验速览

阶段
不适用
入组人数
18,000
试验地点
2
主要终点
HPV infection prevalence

研究概览

简要总结

This is a community intervention effectiveness study in female school students in Thailand.

The study objectives are:

  1. To demonstrate HPV vaccine effectiveness of Single Dose (SD) by a reduction in vaccine-type HPV prevalence (HPV 16 and HPV 18) at Year 2 and Year 4 post vaccination compared to unvaccinated same grade female students
  2. To demonstrate that HPV vaccine effectiveness of SD and two-dose (2D) regimens are similar by comparing reductions in vaccine type prevalence at Year 2 and Year 4 post vaccination compared with the baseline surveys in the two provinces

详细描述

The study will investigate the effectiveness of a SD of HPV vaccine through the conduct of a regional effectiveness study in Thailand.

The study will be conducted in schools and district hospitals from the two selected provinces (Udon Thani and Buriram)

The study design includes 4 distinct and independent components:

  1. vaccination, 2)baseline cross-sectional survey, 3,4)sequential cross-sectional surveys for impact assessments at Year 2 and Year 4 post vaccination.
  • Vaccination: The target population is represented by all Grade 8 female students in the two provinces. All enrolled students will receive either SD (Udon Thani) or 2D (Buriram). A subset (N=200/province) of Grade 8 female students in each province will be selected for a blood collection before vaccination for assessment of vaccine immunogenicity.
  • Surveys (baseline, Year 2 and Year 4 impact surveys): Target populations of are a subset of female students of Grades 10 High school (HS)/year 1 Vocational School (VS) and Grade 12 HS/year 3 VS from all schools in the two provinces and the sampling unit is an individual. Urine collection will be performed to assess HPV infection by DNA PCR and for genotyping of positive samples. A subset of students (N=200 per province) will be randomly selected for each of the Year 2 and Year 4 surveys for blood collection for assessment of vaccine immunogenicity.
  • Demographics and sexual behavior questionnaire will be collected from all students.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
13 Years 至 15 Years(Child)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

HPV infection prevalence

时间窗: Year 4, four years post vaccination

HPV DNA PCR in urine

Identification of HPV circulating strains

时间窗: Year 4, four years post vaccination

HPV genotyping on urine positive samples

次要结局

  • HPV type-specific antibody response prior and post vaccination(Prior vaccination and at Year 2 and Year 4 Post vaccination)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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