Prevention of progression in cervical intraepithelial lesions in patients with HPV Infections and Infestations
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Women diagnosed with low-grade cervical intraepithelial lesions (LSIL) confirmed by colposcopy and histopathological biopsy 2. Age =20 years 3. Positive for human papillomavirus (HPV) infection
Exclusion criteria
Exclusion criteria: 1.Patients with High-Grade Squamous Intraepithelial Lesions (HSIL) , Cervical Cancer, and condylomas 2.Pregnant patients 3. Those who only attended at the beginning and did not return 4. HPV-negative patients at baseline 5. Those who did not sign the informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Regression, persistence, or progression assessed by colposcopic evaluation before and after six months of supplementation measured using patient records | — |
Secondary
| Measure | Time frame |
|---|---|
| Viral load measured by endpoint PCR and optical densitometry before and after six months of supplementation | — |
Countries
Mexico