Patient Reported Outcome on Genital Sensitivity and Sexual Function After Genital Gender Affirming Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-110
SponsorUniversity Hospital, Ghent

About this trial

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.

Eligibility criteria

Qualifiers

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 of 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

Disqualifiers

Absence of signed written informed consent and thus a patient unwilling to participate.

Patient age < 18 years

Cisgender patients

Patients unfit for operation

Trial design

Treatments tested in this trial

  • Semmes-Weinstein monofilament testing and questionnaires

Treatment groups

200 Participants
are divided into 1 treatment group

Sponsors and collaborators