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NCT Number: NCT06082765

Cervical Cancer Screening with NGS-HPV Technology Based on Menstrual Blood

Our study is a population-based, cross-sectional study. This study is conducted to recruit cervical cancer screening participants to evaluate the application value of using high-throughput sequencing technology to detect HPV in menstrual blood for cervical cancer screening. Our study is designed as a two-phase study :

Phase I : This phase, which will be preparing to recruit 5,000 participants, evaluates the accuracy of menstrual blood (MB) self-sampling for detecting cervical intraepithelial neoplasia grade two or worse (CIN2+) in the general population, with a secondary objective to evaluate the Minipad as a special device to collect MB.

Phase II : This phase, which will continue to recruit toward the 10,000-participant target, will evaluate additional molecular markers (specifically DNA methylation) to optimize alternative triage methods for HPV-positive women in menstrual blood (MB) self-sampling. This phase aims to further reduce unnecessary colposcopies while maintaining high sensitivity for CIN2+ detection.

Recruiting

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Key information

Age range

20 year–60 year

Sex eligibility

Female

Study type

Observational

Primary location

Department of Gynecologic Oncology

Wuhan, Hubei, 430062, China

Location status: Recruiting

Location contact

Zheng Hu, doctor

CONTACT

About this study

Our study will recruit 10,000 participants for cervical cancer screening across seven sites in Hubei Province from September 1, 2023, to March 31, 2028. The participating sites include: Fruit Lake Community (where Zhongnan Hospital of Wuhan University is located), Jiang'an District (Wuhan Central Hospital), Huangzhou district of Huanggang County (Huanggang Maternal and Child Health Care Hospital), Jingling Community of Tianmen County (the First People's Hospital of Tianmen), Liutang Community of Huangmei County (Huangmei County People's Hospital), Gongtang Community of Zhongxiang City (Zhongxiang Maternal and Child Health Care Hospital), and Chaihu Community of Zhongxiang City (People's Hospital of Zhongxiang).. The procedures were conducted as below: (1) Conduct cervical cancer screening (TCT+hr-HPV) for all the participants. (2) Collect sanitary napkins from participants during their first menstrual period after cervical HPV testing. (3) Detect HPV using high-throughput sequencing technology in the menstrual blood (MB) from sanitary napkins. (4) Colposcopy referral (biopsy if necessary) for patients with abnormal screening results. (5) Compare the concordance between MB-HPV and clinician-collected HPV. (6) Evaluate the accuracy of menstrual blood (MB) self-sampling for detecting cervical intraepithelial neoplasia grade two or worse (CIN2+) in the general population, with a secondary objective to evaluate the Minipad as a special device to collect MB. (7) Evaluate additional molecular markers (specifically DNA methylation) to optimize alternative triage methods for HPV-positive women in menstrual blood (MB) self-sampling.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • plan to undergo cervical screening
  • with regular menstruation (21-35 days)
  • agree to participate in this study and have signed an informed consent form

Exclusion criteria

  • with amenorrhea or menopause
  • suffering from genital tract infection
  • refuse to participate in this study

Treatment and study plan

Primary outcomes

  1. HPV detection in menstrual blood

    Time frame: December 31, 2025

    In phase I: The primary aim of this study is to evaluate the accuracy of menstrual blood (MB) self-sampling for detecting cervical intraepithelial neoplasia grade two or worse (CIN2+) in the general population.

    In phase II: The primary aim of this study is to evaluate additional molecular markers (specifically DNA methylation) to optimizeThis phase, which will continue to recruit toward the 10,000-participant target, will evaluate additional molecular markers (specifically DNA methylation) to optimize alternative triage methods for HPV-positive women in menstrual blood (MB) self-sampling.

Secondary outcomes

  1. HPV detection in menstrual blood

    Time frame: December 31, 2025

    The secondary objective of this study is to evaluate the accuracy of minipad as a special device for menstrual blood (MB) collection in detecting grade 2 or more cervical intraepithelial neoplasia (CIN2+) in the general population

Study contacts

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

Chen Cao, doctor

CONTACT

[email protected]

+8613986276703

Sponsors and collaborators

Lead sponsor

Zhongnan Hospital

Other

Collaborators

  • Dawu County People's Hospital
  • Gucheng County People's Hospital
  • Guilin People's Hospital
  • Huanggang Maternal and Child Health Hospital
  • Huangmei County People's Hospital
  • Huangmei Maternal and Child Health Care Hospital
  • Jingshan People's Hospital
  • The First People's Hospital of Tianmen
  • Wuhan Central Hospital
  • Wuhan Third People's Hospital
  • Wuxue First People's Hospital
  • Yichang Second People's Hospital
  • Yingshan County People's Hospital
  • Zaoyang Maternal and Child Health Hospital
  • Zhongxiang Maternal and Child Health Hospital
  • Zhongxiang People's Hospital

Registry information

Important dates

Study start
2021
Primary completion
2025
Study completion
2028
First posted
Oct 13, 2023
Registry last updated
Feb 18, 2025

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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