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Clinical Trial Summary

The aim of this post-Market Clinical Follow-up (PMCF) study is to confirm the efficacy and safety of MUCOGYNE® Ovule in the maintainance of natural moisture of the vulvovaginal mucosa and in the compensation for any natural secretions deficiencies, when used in accordance with its approved labeling, in the context of vulvovaginal dryness.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06282614
Study type Interventional
Source Biocodex
Contact Roxane NOEL
Phone +33 3 44 86 75 79
Email r.noel@biocodex.fr
Status Not yet recruiting
Phase N/A
Start date March 2024
Completion date January 2025

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