Probiotc Lactobacillus Crispatus-M247 (Crispact®) Supplementation in the Sterilization of High-risk Human Papilloma (HPV-HR) Viruses

NCT06245486 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2024-02-07

No results posted yet for this study

Summary

There is growing scientific interest in probiotic supplementation as a possible therapy for clearing the human papillomavirus (HPV) infection and reducing the risk of developement of cervical cancer.

Conditions

  • Human Papillomavirus Infection

Interventions

DIETARY_SUPPLEMENT

Crispact®

Contains 20 Bld CFU/Stick of probiotic Lactobacillus crispatus M247

DIETARY_SUPPLEMENT

Placebo

Placebo

Sponsors & Collaborators

  • Università degli Studi dell'Insubria

    collaborator OTHER
  • Liaquat University of Medical & Health Sciences

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-10
Primary Completion
2024-12-31
Completion
2025-03-31

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06245486 on ClinicalTrials.gov