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Clinical Trial Summary

The purpose of this study is to determine whether a formula of boric acid and probiotics for vaginal application is effective in the treatment of symptomatic episodes of vulvovaginitis in comparison to pharmacological reference controls (depending on the suspected diagnosis).


Clinical Trial Description

Multicentre, Open, Prospective, Randomized, Controlled. Women with suspected vaginal infection will be randomized and distributed into two groups (control or boric acid + probiotics). Follow-up will last for three months and consists in 3 visits and a telephone interview. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02860845
Study type Interventional
Source Laboratorios Ordesa
Contact
Status Completed
Phase Phase 4
Start date July 12, 2016
Completion date November 30, 2017

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