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A clinical study on the reversal of Paiteling in cervical HR-HPV infection and low-grade cervical intraepithelial lesions

A clinical study on the reversal of Paiteling in cervical HR-HPV infection and low-grade cervical intraepithelial lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112830
Enrollment
Unknown
Registered
2025-11-20
Start date
2020-12-02
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

HPV infection

Interventions

Experimental Group:The cervix was treated with local application of Petaline

Sponsors

The Second Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
21 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged 21 to 65, with a history of sexual life; 2. The HR-HPV test is positive and has persisted for 6 months or more; 3. Those diagnosed with low-grade cervical intraepithelial lesions or below through colposcopy pathology; 4. No underlying diseases of vital organs; 5. Those who agree to receive treatment and/or follow-up as prescribed and sign the informed consent form; 6. There has been no history of using other cervical drugs in the past three months.

Exclusion criteria

Exclusion criteria: 1.Non-persistent HR-HPV infection; 2. Low immune function or immune system diseases, such as systemic lupus erythematosus (SLE), etc. 3. Currently using immunosuppressants, glucocorticoids and other drugs; 4. Pregnant and lactating women; 5. Acute reproductive tract inflammation; 6. Patients with uncontrolled blood sugar levels due to diabetes; 7. Patients who do not receive full treatment and follow-up; 8. Those who fail to sign the informed consent form; 9. If the researcher assesses and determines that there are any unstable conditions that may affect patient safety and compliance or lead to the forced termination of the study.

Design outcomes

Primary

MeasureTime frame
HPV infection rate;

Secondary

MeasureTime frame
Low grade cervical intraepithelial lesion;

Countries

China

Contacts

Public ContactXuejun Chen

The Second Affiliated Hospital of Zhejiang University School of Medicine

2303011@zju.edu.cn+86 137 5711 9632

Outcome results

None listed

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