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