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Clinical Trial Summary

Patients affected by ASC-US/ low-grade HPV cervical lesions will be randomly assigned to treatment arm vs control arm. The treatment arm will include the characterization of the vaginal microbiota at enrollment (T0), 4 months of oral treatment with Lactobacillus Crispatus M 247 (1 buccal stick Die), characterization of the vaginal microbiota at 1 month post treatment (T5 m). The vaginal microbiota will be evaluated by Danagene microbiome vaginal DNA KIT-XMICROGem (XBIOGem) test, with amplification of the variable regions of the 16S ribosomal RNA gene, using the MICROBIOTA kit (CE-IVD - ARROW diagnostics) and second generation sequencing technologies (NGS on Illumina MiSeq platform). The control arm will provide for the characterization of the vaginal microbiota at the same timescales. Patients will be given a medical history questionnaire at T0 and T5m


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05808816
Study type Interventional
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Rosa Pasqualina RP De Vincenzo, Phd
Phone +0039 3393660390
Email rosapasqualina.devincenzo@policlinicogemelli.it
Status Recruiting
Phase Phase 4
Start date June 16, 2021
Completion date June 30, 2023

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