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RECRUITING
NCT06082765

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

Sponsor: Zhongnan Hospital

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

FEMALE

Age Range

20 Years - 60 Years

Study Type

OBSERVATIONAL

Enrollment

10000

Start Date

2021-09-01

Completion Date

2028-03-31

Last Updated

2025-02-18

Healthy Volunteers

Yes

Conditions

Locations (1)

Department of Gynecologic Oncology

Wuhan, Hubei, China