Skip to main content
Clinical Trials/ISRCTN62596811
ISRCTN62596811Active, not recruiting未知

Effects on cervical high-risk human papillomavirus clearance in patients undergoing treatment with vaginal gel based on carboxy-methyl-beta-glucan in polycarbophil plus an oral probiotic containing L. rhamnosus TOM 22.8 strain: a randomized controlled trial

Ospedale dei Bambini Vittore Buzzi0 sites80 target enrollmentStarted: September 11, 2022Last updated:

Trial Snapshot

Phase
未知
Status
Active, not recruiting
Enrollment
80

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
Female

Inclusion Criteria

  • 1. Women aged 30-45 years
  • 2. Persistent positive cytological LSIL and/or histological CIN 1 and/or HPV HR test for at least 12 months
  • 3. Absence of contraindications to the proposed therapies
  • 4. Read and signed informed consent

Exclusion Criteria

  • 1. Active vulvovaginal infections at the time of their gynaecological examination
  • 2. Genital bleeding of unknown origin
  • 3. Pregnancy
  • 4. Menopause (absence of menstruation for 12 months)
  • 5. Diagnosis of or under therapy for previous CIN2+ lesions
  • 6. Immune-depressed, or with infections caused by human immunodeficiency virus (HIV-positive)
  • 7. Patients concomitantly included in different interventional clinical trials
  • 8. Unwillingness to provide informed consent to the trial

Investigators

Similar Trials