Transcorporal Versus Standard Artificial Urinary Sphincter Placement (TC vs ST AUS)

University of California San Francisco (UCSF)

Status: Terminated

Conditions: Urinary Stress Incontinence

Treatments: Procedure: Artificial Urinary Sphincter Placement

Study type: Interventional

Funder types: Other

Identifiers

NCT02591381

K12DK083021 (U.S. NIH Grant/Contract)

K12DK083021-AUS

Details and patient eligibility

About

The investigators propose a randomized non-blinded comparison of standard vs. transcorporal approach for placement of an artificial urinary sphincter in male patients with stress urinary incontinence after radiation and radical prostatectomy for prostate cancer. In the United States, the artificial urinary sphincter (AUS), manufactured by American Medical Systems, is the gold standard surgical treatment for stress urinary incontinence (SUI) in men. The cuff, which is the portion of the device that encircles and occludes the urethra, is typically placed directly around the urethra (i.e., "standard" placement). The cuff can erode into the urethra. Transcorporal placement has been introduced as a method to reduce the risk of erosion. Transcorporal placement involves tunneling the cuff through the erectile bodies so as to protect the dorsal aspect of the urethra. This approach has never been compared to standard placement in a randomized fashion. In the randomized trial, no additional procedures beyond the normal care protocol will be required of the patients. The investigators will conduct the study through an established, IRB-approved multi-institutional network of surgeons. Success will be assessed via objective and subjective methods; complications will be tallied in a standardized fashion. Outcomes will be measured at two years.

Full description

Procedure/ Methods:

Patients will be identified in the urology clinic upon their standard of care visit for AUS placement. The procedures that determine whether a patient is a surgical candidate are as follows:

• Incontinence Impact Questionnaire Short Form (IIQ-7) and Urinary Incontinence Symptoms index (ISI) standardized questionnaires
• Physical examination
• Review of medical history that would preclude surgery
• Cystoscopy to evaluate and rule out stricture
• Uroflow/Post void residual to ensure adequate bladder capacity

Pre surgery work up includes:

• Urine analysis and if indicated urine culture and treatment of urinary tract infection
• Flow, post-void residual if possible
• Cystoscopy to rule out bladder neck contracture or urethral stricture
• History and physical examination
• Treatment of men with 2 days of chlorhexidine wash to the perineum
• Incontinence sexual function questionaires
• Aminogllycoside and other abx prior to surgery
• 24 hour pad weight

Post-surgery follow up:

• Routine removal of catheter within 5 days post-op
• Treatment of antibiotics post-operatively to be limited to 1 week
• Activation of AUS at 4-8 weeks post-op
• Incontinence sexual function questionnaires
• 24 hour pad weight

Routine follow ups will be conducted at 2 weeks, 6 weeks, 3 months, 6 months post-operatively, and yearly thereafter (SOC). Patient characteristics that will be collected include:

• etiology of the incontinence.
• pre-operative pad usage
• prior anti-incontinence procedures
• adjuvant therapy for prostate cancer such as radiotherapy, or other history of pelvic radiation
• post-operative urodynamic studies
• cystoscopy findings

Enrollment: 3 patients

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• All patients undergoing an AUS procedure would potentially be candidates for the study

Exclusion Criteria: There are several situations in which either a TC or ST procedure would be specifically indicated, and it would be unethical to randomize these patients to the other procedure.

• No men without erectile dysfunction
• No use of injectable agents into the corporal body
• No prior urethral surgery (Prior surgery defined as; urethroplasty, urethral sling, prior AUS placement or explantation, recto-urethral fistula closure)
• No current penile prosthesis
• No concomitant placement of penile prosthesis at the time of AUS placement
• Males under the age of 18, as well as females, are also excluded

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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3 participants in 2 patient groups

STANDARD AUS Placement

Experimental group

Description:

Standard placement of an artificial urinary sphincter involves a small incision made in the patient's perineum or scrotum and a fluid-filled cuff is placed around the bulbar urethra (the portion of the urethra between the bladder neck and penis). Connected to the cuff with tubing, is a balloon filled with fluid that is placed behind the pubic bone or in the space between the peritoneum and abdominal muscles. A control pump is placed in the scrotum and allows the device to cycle, thus either exerting pressure to close off the urethra or releasing pressure to allow the urethra to open and the patient to void.

Treatment:

Procedure: Artificial Urinary Sphincter Placement

TRANSCORPORAL AUS Placement

Experimental group

Description:

Transcorporal placement has been introduced as a way to reduce risk of erosion and involves tunneling the cuff through the erectile bodies. The same incision is made as for the standard approach, and then an incision is made in each corpus cavernosum (cylinders of tissue that allow for erection). This allows the cuff to be placed around both the urethra and through the lining of the corporal bodies, increasing the bulk of tissue behind the urethra to protect it from erosion.

Treatment:

Procedure: Artificial Urinary Sphincter Placement