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Male Stress Urinary Incontinence and Sexual Health

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Stanford University

Status

Withdrawn

Conditions

Prostate Cancer

Treatments

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

Study type

Observational

Funder types

Other

Identifiers

NCT01379378
PROS0035
SU-06152011-7928 (Other Identifier)

Details and patient eligibility

About

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.

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

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).

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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