Recruiting NCT07324967
A Standardized Counseling Approach to Preoperative Education in Transmasculine Individuals Receiving Gender-affirming Surgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Educational Handout.
- Who it may be relevant to
- Registry conditions: Hysterectomy, Gender Affirming Surgery. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The intervention will be an educational handout provided to a randomized cohort of patients that reviews the benefits and risks of retaining ovaries vs removing them. This educational handout will be provided prior to the surgical consultation at the time of the initial survey.
Interventions
- Other Educational Handout
educational handout provided to a randomized cohort of patients that reviews the benefits and risks of retaining ovaries vs removing them. This educational handout will be provided prior to the surgical consultation at the time of the initial survey.
Primary outcome measures
- Decisional Conflict Score [Time frame: Day 1]
Eligibility criteria
Inclusion criteria
- Any transgender or non-binary individual
- Age 18-65
- Assigned female at birth who desires a gender-affirming hysterectomy with or without oophorectomy
- English-speaking
Exclusion criteria
- Non-transgender individuals
- Any transgender individual who has already had a bilateral oophorectomy
- Any transgender person who was born without ovaries or a uterus
- Non-English speaking
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
United States · 1 center
- University of Minnesota — Minneapolis
Identifiers
NCT: NCT07324967 · OBGYN-2025-34532