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Clinical Trial Summary

The investigators are trying to determine if oral Probiotics(Umeta-mimi,30 days) with Metronidazole vaginal suppositories (7 days) is better than using Metronidazole vaginal suppositories(7 days) only in preventing the recurrence of bacterial vaginosis


Clinical Trial Description

Studies have shown that oral Probiotics(Umeta-mimi) can significantly promote the recovery of vaginal flora mainly because intestinal microbiota can migrate and affect vaginal microecology. This project aims to evaluate the efficacy of oral Probiotics(Umeta-mimi,30 days) with Metronidazole vaginal suppositories(7 days) in the treatment of bacterial vaginosis (BV) and to explore the correlation between vaginal flora and fecal flora by detecting the metagenomics of vaginal secretions and intestinal feces at the time of baseline phase,14 days after treatment, the first month after treatment, 5-7 days after third menstruation after treatment and 5-7 days after sixth menstruation after treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04771728
Study type Interventional
Source Peking University Shenzhen Hospital
Contact Shangrong Fan, M.D.
Phone 86-755-83923333
Email fanshangrong@163.com
Status Recruiting
Phase Phase 4
Start date February 1, 2020
Completion date December 1, 2023

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