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Performance and Safety of Class IIb MD Celegyn® in VVA

Vulvovaginal Atrophy Clinical Trial

Official title:
Evaluation of Performance and Safety of the CE Marked Medical Device Class IIb Celegyn® in Vulvovaginal Atrophy (VVA): a Randomised, Double-blind, Parallel Groups, Multicentric, Placebo-Controlled, Prospective Clinical Study

Clinical Trial Summary

The aim of this study is primarily to investigate the performance of Celegyn®, a hyaluronic acid-based vaginal cream (CE marked 0546 medical device), enriched with plant-based ingredients, in comparison with placebo, in promoting vaginal health in adult woman reporting symptoms of vulvovaginal atrophy - VVA (or atrophic vulvovaginitis)

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03823560
Study type Interventional
Source Nathura S.p.A
Contact Antonio Bertolino, PhD
Phone +390249530065
Email antonio.bertolino@evidilya.com
Status Recruiting
Phase N/A
Start date September 24, 2019
Completion date September 2021
View Details
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