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Analysis of Risk Factors for Persistent HR-HPV Infection in HSIL Patients after Cervical LEEP Procedure

Analysis of Risk Factors for Persistent HR-HPV Infection in HSIL Patients after Cervical LEEP Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114955
Enrollment
Unknown
Registered
2025-12-19
Start date
2025-12-30
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical intraepithelial neoplasia grade II, cervical intraepithelial neoplasia grade III, cervical carcinoma in situ, high-risk human papillomavirus (HR-HPV) infection

Interventions

persistent HR-HPV infection group:None
HR-HPV negative conversion group:None

Sponsors

The International Peace Maternity and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Underwent cervical loop electrosurgical excision procedure (LEEP) at our hospital's cervical clinic, with preoperative colposcopy-directed biopsy or postoperative LEEP pathology confirming high-grade cervical intraepithelial neoplasia (HSIL, CIN2, or CIN3); 2. Completed HR-HPV genotyping tests both before and after surgery, with at least one positive HR-HPV result, and with traceable laboratory test results; 3. Postoperative follow-up of at least 18 months, with at least 2 follow-up visits (each including HPV genotyping and cervical cytology re-examination); 4. Complete clinical data, including age, menopausal status, obstetric history, cervical cytology, colposcopic findings, pathology results, and postoperative follow-up information.

Exclusion criteria

Exclusion criteria: 1.incomplete key information (e.g., negative preoperative HPV, unknown HPV genotyping, interrupted follow-up or loss to follow-up; 2.Patients who underwent total hysterectomy, cervical cryotherapy, laser therapy, photodynamic therapy, or other local adjuvant therapies within 6 months after cervical LEEP; 3.Patients who underwent LEEP during pregnancy or within 8 weeks postpartum; 4.A history of invasive cervical treatment (including LEEP, conization, cryotherapy, or laser therapy) in the past; 5.A previous diagnosis of cervical cancer or other malignant tumors of the reproductive tract; 6.A history of pelvic radiotherapy or systemic chemotherapy; 7.Long-term use of immunosuppressants or complicated with immune system diseases (e.g., systemic lupus erythematosus, HIV infection, etc.

Design outcomes

Primary

MeasureTime frame
Infection status of different HR-HPV types after cervical LEEP surgery ;

Secondary

MeasureTime frame
High-risk factors for disease residue or recurrence in patients after cervical LEEP surgery;

Countries

China

Contacts

Public ContactWang Liya

The International Peace Maternity and Child Health Hospital

annya1985010@sina.com+86 10 64070434

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026