Sustainability of Vaginal Estrogen Therapy in Postmenopausal Women

Status Completed

Clinical Trial Summary

Sustainability of vaginal ultra-low dose estrogen therapy in postmenopausal women

Clinical Trial Description

Within this trial 50 postmenopausal women receive a vaginal estrogen therapy as treatment for symptomatic vaginal atrophy. The sustainability of vaginal estrogen therapy after the end of therapy has not yet been investigated. All participants will be asked to come for the following 7 visits. - Visit 1: Standard Gynecological examination; Inclusion and exclusion criteria check - Visit 2: Handing out of Gynoflor (estrogen) for a 6 weeks treatment. - Visit 3 (Study Start): After using the vaginal estrogen for 6 weeks, a vaginal swap will be done to measure the vaginal maturation index (VMI). The participants will also receive a questionnaire to define some subjective parameters. The parameters measured at visit 1 will count as reference. The estrogen therapy will now be sustained. - Visit 4-6: Measuring of the VMI and handing out the questionnaires to define subjective parameters. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02887885
Study type	Observational
Source	University Hospital Inselspital, Berne
Contact
Status	Completed
Phase
Start date	January 22, 2018
Completion date	April 10, 2020

View Details

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