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Clinical efficacy safety and mechanism of a traditional chinese medicine of Capilliposide vaginal gel for cervical squamous intraepithelial lesion

Clinical efficacy and mechanism of a traditional chinese medicine of Capilliposide vaginal gel for cervical squamous intraepithelial lesion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002151
Enrollment
Unknown
Registered
2025-11-08
Start date
2023-03-29
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Cervical Squamous Intraepithelial Lesion

Interventions

Safety Evaluation Group:Bijieshu female antibacterial gel
Therapeutic effect evaluation group:Bijieshu female antibacterial gel

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 74 Years

Inclusion criteria

Inclusion criteria: (1) a biopsy-confirmed tissue diagnosis of CIN1/2/3 (2) HPV infection and (3) agreement and ability to comply with the study protocol requirements.

Exclusion criteria

Exclusion criteria: (1) allergy to CVG (2) patients with unsatisfactory colposcopy (3) history of invasive cervical carcinoma or other invasive malignancies (4) presence of skin and mucosal infections or overt pyometra (5) acute inflammation of the female reproductive tract (6) pregnancy or breastfeeding (7) Other serious conditions that may significantly affect compliance with clinical studies such as unstable heart disease requiring treatment kidney disease chronic hepatitis poorly controlled diabetes and mental illness.

Design outcomes

Primary

MeasureTime frame
The condition of SIL turning negative;

Secondary

MeasureTime frame
safety;HPV results;

Countries

China

Contacts

Public ContactHanmei Lou

Zhejiang Cancer Hospital

louhm@zjcc.org.cn13355783145

Outcome results

None listed

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