Clinical Trial

Peripheral Blood CyTOF Immune Model for Cervical Lesion Detection in HPV16/18+ Women

Not Yet Recruiting
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Summary
This prospective, multicenter cohort study will recruit eligible HPV16/18-positive women from three tertiary hospitals in China. Peripheral blood samples and clinical data (cytology, HPV genotyping, colposcopy-directed biopsy) will be collected, followed by standardized mass cytometry (CyTOF) to develop and evaluate an immune model across cervical lesion grades.
Trial Details
NCT Number NCT07606677
Lead Sponsor Women's Hospital School Of Medicine Zhejiang University
Collaborators: Jiaxing Maternity and Child Health Care Hospital, Ningbo Women & Children's Hospital, Zhejiang PuLuoTing Health Technology Co., Ltd.
Conditions CIN 2/3, Cervical Cancer (Early Detection)
Enrollment 1,465 participants
Start Date 2026-05-15
Primary Completion 2027-03-31 (estimated)
Study Completion 2028-03-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-26