The effect of topical Imiquimod5% in treatment of high-grade cervical neoplasias (CIN2,3)
Phase 3
- Conditions
- The recovery rate of high-grade cervical neoplasias.
- Registration Number
- IRCT20230811059116N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
Age 20-45 years old
Diagnosis of high-grade cervical neoplasia (CIN2,3)
Obtaining informed consent
Exclusion Criteria
Cortone therapy
Pregnancy
Suppressed immune system due to HIV or organ transplant
Prior treatment for HSI
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cervical intraepithelial neoplasia (CIN). Timepoint: 12 weeks after using topical imiquimod cream5%. Method of measurement: Loop Electrosurgical Excision Procedure and histological examination.
- Secondary Outcome Measures
Name Time Method