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临床试验/NCT07468578
NCT07468578尚未招募不适用

Community Implementation of Urine HPV Test and Reflex DNA Methylation Test in Cervical Cancer Screening

The University of Hong Kong1 个研究点 分布在 1 个国家目标入组 8,620 人开始时间: 2026年4月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
8,620
试验地点
1
主要终点
To explore the effectiveness of urine self-sample HPV test as screening tool in cervical cancer screening

研究概览

简要总结

Aims:

The project aims to explore the acceptability and feasibility of a self-sampling, urine-based HPV test (INDICAID HPV Urine Test) in a community setting, and the effectiveness of DNA methylation test for triaging high-risk HPV (HR-HPV) positive women to colposcopy examination compared to the current standard triage methods of cytology and HPV16/18 genotyping.

There are two main hypotheses:

  1. Urine self-sampling for HPV testing is an acceptable cervical screening option for women in the community.
  2. Combining urine HPV testing with DNA methylation will increase the detection rate of high-grade lesions without increasing the colposcopy referral rate.

Target participants:

Women between the ages of 26-65 and have a history of sexual activity, not have a history of total hysterectomy or cervical cancer, not currently pregnant, not currently under treatment of cervical dysplasia or cervical cancer.

This is a prospective study and women who are willing to undergo urine self-sampling for HPV test will be recruited from various communities, such as Specialist out-patient clinics of Queen Mary Hospital (Hong Kong), public areas in Queen Mary Hospital (such as lobby of out-patient clinics and corridors), District Health Centres, the Family Planning Association (FPA) clinics, Anticancer Society, Christian Action, Non Government Organizations (NGO), private organizations, and online.

A total of 8,620 women are needed to be recruited to the study: approximately 4,700 onsite and 4,000 online.

Study procedures:

Self-collected urine samples from study subjects recruited in various communities will be examined using the INDICAID HPV Urine Test. Women with positive urine HPV results will undergo further testing, including urine DNA methylation and co-testing (cytology and HPV genotyping). They will be triaged to colposcopy when test results show clinical indications. The acceptability and feasibility of the urine test will be assessed by calculating the self-sample uptake rate and analyzing participant-reported questionnaires. The detection rate of high-grade lesions and the colposcopy referral rate will be compared between DNA methylation testing and the current standard methods.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
26 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Women aged 26-65
  • History of sexual activity

排除标准

  • Pregnancy
  • History of total hysterectomy
  • History of cervical cancer
  • Currently under treatment for cervical dysplasia or cervical cancer
  • Unwilling to participate in the study
  • Cannot give written consent to the procedure

结局指标

主要结局

To explore the effectiveness of urine self-sample HPV test as screening tool in cervical cancer screening

时间窗: through study completion, an average of 18 months

Comparison of high-grade squamous intraepithelial lesion (HSIL) detection rate and colposcopy referral rate by different triaging methods: cytology, HPV16/18 genotyping or DNA methylation test.

次要结局

  • To explore the feasibility of urine self-sample HPV test in community application(15 months)
  • To explore the acceptability of urine self-sample HPV test in community application(15 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Karen Kar Loen CHAN

Clinical Professor and Department Chairperson

The University of Hong Kong

研究点 (1)

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