Hysterectomy Clinical Trials

Clinical trials related to Hysterectomy Procedure

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

Status: Recruiting
Location: See location...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

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
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
United States
Rhode Island
Women & Infants Hospital
RECRUITING
Providence
Contact Information
Primary
Beth Cronin, MD
bcronin@wihri.org
401-274-1122
Time Frame
Start Date: 2025-05-01
Estimated Completion Date: 2026-12-01
Participants
Target number of participants: 48
Treatments
Placebo_comparator: Placebo
Standard surgical treatment will be provided
Experimental: Estradiol
Application of topical estradiol at conclusion of surgery
Related Therapeutic Areas
Sponsors
Leads: Women and Infants Hospital of Rhode Island

This content was sourced from clinicaltrials.gov