Actively Recruiting
ZEPHYR: A Study Evaluating Surgical Outcome After Implantation of the Zephyr ZSI 475 FTM Inflatable Penile Implant in the Neophallus After Female-to-male Sex Reassignment Surgery
Led by University Hospital, Ghent · Updated on 2024-01-30
100
Participants Needed
1
Research Sites
636 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study will look into the surgical outcome after implantation of the Zephyr ZSI 475 FTM in the neophallus.
CONDITIONS
Official Title
ZEPHYR: A Study Evaluating Surgical Outcome After Implantation of the Zephyr ZSI 475 FTM Inflatable Penile Implant in the Neophallus After Female-to-male Sex Reassignment 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.
- Age 63 18 years.
- Female-to-male transsexual patient.
- Implantation of Zephyr ZSI 475 FTM erectile device.
You will not qualify if you...
- Absence of signed written informed consent.
- Age < 18 years.
- Biological males.
- Patients opting for penile implants other than the Zephyr ZSI 475 FTM.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Urology, Ghent University Hospital
Ghent, Oost-Vlaanderen, Belgium, 9000
Actively Recruiting
Research Team
W
Wesley Verla
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
0
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