Effectiveness of HPV Vaccine Among Women Age Equal or More Than 20 Years
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 993
- 试验地点
- 5
- 主要终点
- Occurrence of Low-grade squamous intraepithelial lesion or worse (LSIL+) associated with HPV 16 or 18
研究概览
简要总结
- Background: The majority of the burden of HPV-related cervical cancer is in developing countries while most of the effectiveness reports of HPV vaccination are currently coming from developed countries. Also, currently many adult women are left without either HPV vaccination or cervical cancer screening. Effectiveness data of currently available HPV vaccines among adult women in developing countries are needed for women and healthcare workers and policy makers to best protect women from cervical cancer.
- Primary Study Objective:
- To determine the effectiveness bivalent and quadrivalent HPV vaccines in reduction of cervical dysplasia (Low-grade Squamous Intraepithelial Lesion or worse; LSIL+) attributable to HPV types 16 or 18 after at least 5 years of vaccination among Thai women vaccinated at their ages 20-45 years with at least one dose of the HPV vaccine
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Secondary Study Objectives:
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To measure the effectiveness of currently available bivalent and quadrivalent HPV vaccines in reducing the prevalence of HPV 16 or 18
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To measure the effectiveness of HPV vaccines in reducing any abnormal Pap smear result (ASC-US+)
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To compare the effectiveness of HPV vaccines according to the number of doses immunized
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To find out risk factor(s) for HPV 16 or 18-related cervical dysplasia in this cohort
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To assess the prevalence of other high-risk HPV types in vaccinated and non-vaccinated group
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To determine direct and/or indirect cost of HPV vaccination
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The hypothesis to be tested: At least one dose of vaccination with bi- or quadri-valent HPV vaccine will reduce the prevalence of LSIL+ attributable to HPV 16/18 by 80% after at least 5 years of vaccination.
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Materials and Methods: This study will be a retrospective matched cohort study. Data is to be collected either by from samples for Pap and HPV test and/or HPV 16/18 genotyping of the recruited participants, or from existing medical records. HPV vaccinated women at their ages 20-45 years (vaccinated group) and women received Pap smear at their ages 20-45 years without vaccination (control group) will be included in the study. Pap smear and HPV test and/or HPV 16/18 typing result of 2 groups will be compared after ≥ 5 years of vaccination or baseline Pap smear. Those who don't have Pap smear results ≥ 5 years after vaccination or ≥ 5 years after the baseline Pap smear will be offered for a Pap smear and HPV 16/18 typing
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 25 Years 至 53 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- •Known pregnancy
- •History of hysterectomy or excisional treatment of the cervix
- •Known increased risk of bleeding
- •Not willing to provide written informed consent
结局指标
主要结局
Occurrence of Low-grade squamous intraepithelial lesion or worse (LSIL+) associated with HPV 16 or 18
时间窗: Sample collection in the project is single 1 day time for participants who received vaccination at least 5 years ago.
LSIL or worse, including Atypical Glandular Cells, High-grade squamous intraepithelial lesion, Cervical intraepithelial neoplasia (CIN) grade 1-3, and cervical cancer which are associated with either HPV 16 or 18
次要结局
- Cost-effectiveness of bivalent and quadrivalent HPV vaccination(Interview for direct and indirect cost survey will be single 1 day time for a participant.)