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A Clinical Efficacy Study of Photodynamic Therapy for Cervical Intraepithelial Neoplasia

A Clinical Efficacy Study of Photodynamic Therapy for Cervical Intraepithelial Neoplasia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127297
Enrollment
Unknown
Registered
2026-06-29
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

CIN1?CIN2

Interventions

Observation group:None

Sponsors

Guangdong Province Hospital for Women and Children Healthcare
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1.Patients with persistent HR-HPV infection for more than 1 year and pathological diagnosis of CIN 1 in cervical biopsy before treatment; 2.CIN 2 patients aged 20-35 years old who want to have children, the cervical transformation zone and the upper edge of the lesion are completely visible under colposcopy, and there is no HSIL, invasive cancer or glandular epithelial lesions in the cervical canal. 3.Have complete follow-up data;

Exclusion criteria

Exclusion criteria: 1. Patients whose pathological diagnosis is suspected or confirmed to be CIN 3 or higher, carcinoma in situ of the cervix, or invasive cervical cancer; 2. Patients with cytology results showing atypical glandular cells (AGC), atypical glandular cells favoring neoplasia (AGC-FN), cervical adenocarcinoma in situ (AIS), adenocarcinoma (AC), or suspected malignancy; 3. Patients with other reproductive tract malignancies; 4. Patients who are pregnant or breastfeeding; 5. Patients with immune system diseases, HIV infection, or who have been on long-term immunosuppressants in the past 3 months; 6. Patients with severe systemic diseases like heart, liver, or kidney failure who cannot tolerate treatment; 7. Patients with uncontrolled acute reproductive tract infections at the time of treatment; 8. Patients known to be allergic to the photosensitizer or its analogs, or who have porphyria, photosensitive disorders, or sunlight-related dermatitis; 9. Patients lost to follow-up or with incomplete clinical data.

Design outcomes

Primary

MeasureTime frame
Remission of lesions;High-risk HPV remission status;

Countries

China

Contacts

Public ContactLi Zhimin

Guangdong Province Hospital for Women and Children Healthcare

439622534@qq.com+86 20 3915 1611

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026