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HYDEAL-D® Application for Promoting the Restoration of Sexual Function in the Postpartum Period — HYDEAL-D  

Sexual Dysfunction Clinical Trial

Official title:
Randomized Clinical Trial to Assess the Efficacy and Safety of HYDEAL-D® Application in Promoting the Restoration of Sexual Function in the Postpartum Period

Clinical Trial Summary

During postpartum and lactation, vaginal epithelium tends to have an impaired degree of hydration and lubrication. This may lead to vaginal dryness, burning sensation dyspareunia or itching, which negatively affect the sexual function of puerperal women. This study aimed to evaluate the efficacy of HYDEAL-D® vaginal gel (HYALOGYN®, Fidia Farmaceutici, Abano Terme, Italy) application on promoting the restoration of sexual function in the postpartum period.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04560283
Study type Interventional
Source Ospedale Policlinico San Martino
Contact
Status Completed
Phase Phase 4
Start date September 1, 2016
Completion date September 1, 2020
View Details
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