Antisepsis Regimen in the Surgical Treatment of Human Papilloma Virus Generated Cervical Lesions: Polyhexamethylene Biguanide Versus Chlorhexidine

Antisepsis Regimen After Surgical Treatment of HPV Infected Lesions Clinical Trial

Status Completed

Clinical Trial Summary

Treatments for the macroscopic or pathologic lesions caused by HPV infection can be classified as topical, surgical, destructive, or immunomodulatory. Post surgical treatments generally consist of analgesic, anti-inflammatory and topical antimicrobial agents to reduce the risk of local infections.

The aim of this study is to compare the efficacy and safety of polyhexamethylene biguanide-based vaginal suppositories to a similar chlorhexidine-based treatment, in the post recovery regimen after surgical treatment of cervical lesions.

Women who underwent to CO2 laser therapy for cervical lesions are randomly assigned to receive 10 days of antiseptic treatment with chlorhexidine digluconate vaginal suppositories, or polyhexamethylene biguanide vaginal suppositories (Monogin® / BiguanelleTM vaginal suppositories, Lo.Li.Pharma, Italy). A weekly follow-up check was performed for 6 weeks.

Clinical Trial Description

n/a

Study Design

N/A

Related Conditions & MeSH terms

• Antisepsis Regimen After Surgical Treatment of HPV Infected Lesions

• NCT number: NCT01740245
• Study type: Interventional
• Source: AGUNCO Obstetrics and Gynecology Centre
• Status: Completed
• Phase: Phase 4