Topical Estrogen: Brief Intervention to Improve Postoperative Experience for Transgender Men Undergoing Hysterectomy

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWomen and Infants Hospital of Rhode Island

About this trial

The purpose of this study is to determine if applying a single dose of topical estrogen cream in the operating room at the end of your hysterectomy (removal of uterus and cervix) improves the postoperative experience with bleeding and potential symptoms of dysphoria (a feeling of discomfort or distress). Topical estrogen cream is sometimes used if patients have increased risk of bleeding with surgery but is not currently utilized in a consistent way. This study aims to answer the question of whether this is a helpful treatment and should be included in standard postoperative care.

Eligibility criteria

Qualifiers

Gender diverse/transgender men

Age 18 or older

Have been on testosterone for at least 6 months with plan to undergo gender-affirming hysterectomy and are willing to be randomized to the use of topical estrogen postoperatively.

Have stable physical and mental health

Disqualifiers

Under age 18

Have not been on testosterone for at least 6 months prior to planned hysterectomy

Known allergy to topical estrogen

Trial design

Treatments tested in this trial

  • Use of topical estradiol
  • No intervention

Treatment groups

48 Participants
are divided into 2 treatment groups