Trial Search Results

Male Stress Urinary Incontinence and Sexual Health

The purpose of this study if to demonstrate if post-prostatectomy incontinence is a barrier to sexual satisfaction/frequency/desire and if surgical correction of incontinence will improve these aspects of sexual health.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Stanford University

Stanford Investigator(s):


  • Device: Artificial urinary sphincter
  • Device: InVance Sling
  • Device: AdVance Sling
  • Device: Virtue Sling
  • Drug: Contigen


Inclusion Criteria:

   - Adult men age 18-80 who have had an open or laparoscopic radical prostatectomy more
   than 6 months ago who have bothersome urinary incontinence.

Exclusion Criteria:

   - Any significant cardiac or pulmonary co-morbidities that would preclude the patient
   from another surgical procedure as they would be too high risk for general anesthesia.

   - They will also be excluded if based on their anatomy or urodynamics, they will most
   likely not benefit from a surgical incontinence procedure (e.g. poor bladder
   contractility, bladder neck contracture, etc).

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Patricia Glowe