Actively Recruiting
Cervical and Endometrial Cancer Screening in Patients Seeking Gender-Affirming Hysterectomy
Led by University of Minnesota · Updated on 2025-07-20
40
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to quantify the rates of cervical cancer screening and endometrial sampling prior to gender-affirming hysterectomy, assess the need for these tests in TGD individuals, and explore patient-centered options for these tests. By assessing the status of testing and correlation with hysterectomy pathology, this study will provide preliminary data on the current state of guideline-concordant care and provide initial evidence for the development of evidence-based guidelines in the future
CONDITIONS
Official Title
Cervical and Endometrial Cancer Screening in Patients Seeking Gender-Affirming Hysterectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years and older
- Able to provide voluntary written consent prior to the performance of any research related activity
- Able to understand, speak, read, and write in English
- Patients who have undergone hysterectomy, or plan to have a hysterectomy
- Patients who are transgender and gender diverse
You will not qualify if you...
- Opted out of research
- Younger than 18 years old
- Lacks capacity or has diminished capacity to consent
- Cannot provide informed consent
- Those on the study's community advisory board
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneota, Minnesota, United States, 55455
Actively Recruiting
Research Team
M
Maria Bunch
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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