3D Models for Vaginoplasty Education and Outcomes

This study is looking at whether using 3D printed models of your own body can help you better understand gender-affirming peritoneal vaginoplasty (a type of surgery to create a vagina). Researchers want to see if these models improve patient education, communication with doctors, and potentially lead to better surgical results like shorter operating room times and fewer complications. You might be able to join if you are an adult assigned male at birth (AMAB), are at least 18 years old, have been diagnosed with gender dysphoria, are seeking vaginoplasty, and can give consent in English. The study aims to enroll 20 participants. Success will be measured by how well you understand the surgery after using the 3D models.

Study design
This is an observational study involving 20 participants. It is not specified if it is randomized or blinded.
What's involved
You would use 3D printed patient-specific models for education during a baseline visit. Your understanding of the surgery will be measured immediately after this visit.
Compensation
Not stated in the trial record.
Follow-up
Your understanding will be measured immediately after the baseline visit. No further follow-up is specified.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07412509

Can 3D Modeling Enhance Patient Understanding, Education, and Surgical Outcomes in Gender Affirming Peritoneal Vaginoplasty?

Not Yet Recruiting
Not specifiedAges 18+Observational
University of Chicago
~20 participants
Updated 2026-04-21 on ClinicalTrials.gov
What's tested:Use 3D printed patient specific models for patient education

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Use of 3D-printed patient-specific models for patient education
Measured over Baseline
+1 more outcome measured
Vaginoplasty
Gender Dysphoria, Adult
1 sites across 1 states
Illinois1

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Have a diagnosis of gender dysphoria
Seeking Vaginoplasty
Able to provide electronic informed consent in English

Exclusion

Vulnerable subjects (children, prisoners, pregnant women) will be excluded Participants may withdraw from this study for any reason at any point by actively asking a research team member. All investigations and standard clinical care will be performed at the main campus of The University of Chicago Medicine at 5841 S. Maryland Ave. in Chicago, IL.
  • Use of 3D-printed patient-specific models for patient educationBaseline

    To use 3D printing to generate patient-specific models of abdominal and pelvic anatomy to educate patients about the procedure, including risks, benefits, and potential complications.

  • Participant-reported understanding of gender-affirming vaginoplasty following use of 3D models.immediately after baseline visit

    To evaluate participant knowledge and satisfaction with use of 3D Models for discussing Gender- affirming vaginoplasty surgery.