Effect of supplementation in treatment of women with cervical intraepithelial neoplasia 2 and 3
Phase 3
- Conditions
- C53.9Cervical intraepithelial neoplasia 2 and 3.Cervix uteri, unspecified
- Registration Number
- IRCT201601045623N65
- Lead Sponsor
- Vice chancellor for research, Kashan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 58
Inclusion Criteria
Women with cervical intraepithelial neoplasia 2 and 3
Aged 25 to 65 years old
Exclusion Criteria
Women who had a history of cervical cancer or other cancers of the lower genital tract
History of hysterectomy or destructive therapy of the cervix
Pregnant women
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Recurrence. Timepoint: Six months after intervention. Method of measurement: Colposcopy.
- Secondary Outcome Measures
Name Time Method