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NCT Number: NCT07468578

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

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.

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Key information

Age range

26 year–65 year

Sex eligibility

Female

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women aged 26-65
  • History of sexual activity

Exclusion criteria

  • 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

Treatment and study plan

Primary outcomes

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

    Time frame: 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.

Secondary outcomes

  1. To explore the feasibility of urine self-sample HPV test in community application

    Time frame: 15 months

    Uptake rate of the urine self-sample HPV test (calculated by the number of samples returned/the number of self-samples bottle distributed).

  2. To explore the acceptability of urine self-sample HPV test in community application

    Time frame: 15 months

    Acceptability of the urine self-sample HPV test in cervical cancer screening by questionnaires survey

Study contacts

Contact information is provided by the study sponsor or research team.

Karen Kar Loen Prof CHAN, MBBChir (Cantab); MD (HK)

CONTACT

[email protected]

852-22554265

Tina Na Dr WEI, PhD

CONTACT

[email protected]

852-22554265

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Collaborators

  • Innovation and Technology Commission, Hong Kong
  • Phase Scientific International Limited

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Mar 12, 2026
Registry last updated
Mar 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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