Topical Estrogen: Brief Intervention to Improve Postoperative Experience for Transgender Men Undergoing Hysterectomy
Recruiting now · Phase 3 · Has a placebo group
Conditions studied: Postoperative Bleeding, Gender Dysphoria, Hysterectomy
In brief
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.
Key facts
- Study ID
- NCT06969326
- Run by
- Women and Infants Hospital of Rhode Island
- People needed
- 48
- Starts
- 2025-05-01
- Expected to finish
- 2026-12-01
- Last updated by the study team
- 2025-05-13
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- 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
- No contraindications to estrogen therapy
- Must be proficient in English or Spanish
- Must have access to a device to receive text messages for study follow up
- Must agree to allow their medical data to be used for research purposes
You may not qualify if…
- Under age 18
- Have not been on testosterone for at least 6 months prior to planned hysterectomy
- Known allergy to topical estrogen
Where it is running
- Women & Infants Hospital — Providence, Rhode Island, United States (enrolling)
Full record on ClinicalTrials.gov
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