Urethral Sterilization With Chlorhexidine Digluconate to Facilitate Primary Repair & Same-Session Implantation
Status:
Unknown status
Trial end date:
2018-12-01
Target enrollment:
Participant gender:
Summary
The introduction of penile implants has revolutionized the management of male erectile
dysfunction. However, a number of intraoperative complications may occur, which have a major
impact on clinical outcomes and patient satisfaction such as bleeding, infection and urethral
injury.
Patients undergoing penile implant surgery with fibrotic corpora (e.g., after priapism, after
infection, or with Peyronie disease) have a higher risk rates of urethral perforation. This
may be related to previous scarring, the difficultly in dilating scarred and fibrotic corpora
and its inherent risk of corporal crossover and urethral perforation.
This work examines the efficacy of pre-operative urethral sterilization in rendering the
urethra as sterile as the skin of the genital area, with the skin sterilized as per the ISSM
guidelines for penile prosthesis implantation, thereby allowing primary repair of urethral
injuries should they occur, and implantation in the same setting, without a higher risk of
infection.
The study will involve 100 male patients undergoing aseptic surgery (regardless the
procedure). Patients will be divided into two groups:
Group 1: control group, n=50 Group 2: Chlorhexidine group (Ch group), n=50 Pre-operatively,
urethral instillation with Chlorhexidine gel will be performed for the Ch group, while for
the control group, instillation will not be performed.
After conclusion of surgery and with the patient on the operative table, the following swabs
will be obtained:
- A penile skin swab.
- A urethral swab. Skin and urethral swabs will be compared for bacterial colonization by
culture and sensitivity, across the two groups.