About this trial

To analyze the short and long term postoperative clinical outcome and patient satisfaction of silicone gel-filled testicular implants.

Eligibility criteria

Qualifiers

The patient is an adult or a child at the time of testicular implant placement.

The patient is a candidate to unilateral or bilateral testicular implant placement.

The patient has been informed of the study, has read the patient information letter and provided oral and written consent.

If the patient is of French nationality, he/she must be affiliated to the French Social Security.

Disqualifiers

The patient has silicone implants somewhere else than in the scrotal sac (except for a penile prosthesis).

Trial design

Treatments tested in this trial

  • Placement of testicular prosthesis

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

1
University Hospital Ghent9000, GhentEast-Flanders, Belgium

Sponsors and collaborators

University Hospital, Ghent

Lead sponsor

Groupe SEBBIN

Collaborator