Actively Recruiting
Patient Reported Outcome on Genital Sensitivity and Sexual Function After Genital Gender Affirming Surgery
Led by University Hospital, Ghent · Updated on 2023-12-22
200
Participants Needed
1
Research Sites
500 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
For genital gender affirming surgery, it remains unclear to what extent genital sensitivity might be expected and what the impact of this might be on sexual functioning.
CONDITIONS
Official Title
Patient Reported Outcome on Genital Sensitivity and Sexual Function After Genital Gender Affirming Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Voluntarily signed written informed consent according to the rules of Good Clinical Practice (Declaration of Helsinki) and national regulations
- Patient age 18 years
- Transgender male, female or gender non-conforming patient with diagnosed gender dysphoria and the specific wish to undergo genital gender affirming surgery
- Fit for operation, based on the surgeon's expert opinion
- Patient is able and willing to attend the follow-up consultations
You will not qualify if you...
- Absence of signed written informed consent and thus a patient unwilling to participate
- Patient age < 18 years
- Cisgender patients
- Patients unfit for operation
- Patient declares that it will be impossible for him to attend the follow-up consultations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital Ghent
Ghent, East-Flanders, Belgium, 9000
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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