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Study identifier: NCT06639776 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Sexual Functioning After Erection Prosthesis Placement in Post Phalloplasty Transgender Persons

Condition: Transgenderism · Erectile Dysfunction · Prosthesis Durability  ·  Sponsor: University Hospital, Ghent

PhaseN/A
Planned participants150
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to explore sexual satisfaction among transgender men and their partners following the placement of erectile prostheses after phalloplasty. While phalloplasty can create a neophallus, the lack of natural erectile tissue often necessitates the use of erectile aids, including internal prostheses. However, these prostheses, originally designed for cisgender men, face challenges when used in transgender patients, such as higher risks of complications, infections, and mechanical failures. Despite these issues, some studies report high patient satisfaction, though partner satisfaction rates are significantly lower. The study will use validated and non-validated questionnaires to assess satisfaction with various types of erectile prostheses, addressing the gap in understanding how these devices impact the sexual and relational functioning of both transgender men and their partners. These questionnaires will be provided to all included patients that are minimum 6 months after placement of an internal erection prosthesis and have a functional erection prosthesis in place

This description comes directly from the study's public registry record.

Talk to the study team

Wietse Claeys, MD  ·  003293322276  ·  wietse.claeys@ugent.be

Anne-Françoise Spinoit, MD, PhD  ·  003293322276  ·  anne-francoise.spinoit@uzgent.be

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Urology, University Hospital GhentGhent, East-Flanders, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT06639776