Difference in Serum Estrogen Level Based on Methods of Vaginal Estrogen Application (fingertip Vs Applicator Use) in Post-menopausal Women

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexFemale
Age18-100
SponsorWalter Reed National Military Medical Center

About this trial

Study the change in serum estrogen level based on the method of vaginal cream application (applicator vs fingertip application) and Measure patient satisfaction with vaginal estrogen cream application based on the method of application using a validated patient questionnaire (Likert scale).

Eligibility criteria

Qualifiers

patients who are postmenopausal for at least 1 year (since their last menses)

patients who qualify for treatment with vaginal estrogen cream and are willing to complete the treatment

English speaking patients

patients should be able to self-apply the vaginal estrogen cream using the applicator method and the fingertip application

Disqualifiers

pre and perimenopausal women

contraindication to estrogen therapy (Deep vein thrombosis, history or active cancer)

women who are not able to self apply the vaginal estrogen cream

vaginal bleeding of unknown origin

Trial design

Treatments tested in this trial

  • application of the vaginal estrogen cream

Treatment groups

110 Participants
are divided into 2 treatment groups

Locations

This trial has no locations