Transcorporal Versus Standard Artificial Urinary Sphincter Placement

Urinary Stress Incontinence Clinical Trial

— TC vs ST AUS  

Official title:

A Randomized Study of Transcorporal Versus Standard Artificial Urinary Sphincter Placement

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02591381
• Other study ID #: K12DK083021-AUS
• Secondary ID: K12DK083021
• Status: Terminated
• Phase: N/A
• Start date: October 2015
• Est. completion date: October 2017

Study information

• Verified date: May 2018
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

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

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. completion date: October 2017
• Est. primary completion date: October 2017
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Urinary Incontinence, Stress
• Urinary Stress Incontinence

Intervention

Procedure:
• Artificial Urinary Sphincter Placement
The AUS is the gold standard for treatment of severe stress urinary incontinence, particularly in patients following surgical resection of the prostate for prostate cancer. AUSs are small devices that prevent urinary flow via compression of the urethra, thus mimicking the native urinary sphincter.

Locations

Country	Name	City	State
United States	University of California San Francisco	San Francisco	California

Sponsors (12)

Lead Sponsor	Collaborator
University of California, San Francisco	Baylor College of Medicine, Central Ohio Urology Group, Lahey Clinic, Loyola University Chicago, New York University, University of California, San Diego, University of Iowa, University of Kansas, University of Minnesota - Clinical and Translational Science Institute, University of Utah, University of Washington

Country where clinical trial is conducted

United States, 

References & Publications (4)

Aaronson DS, Elliott SP, McAninch JW. Transcorporal artificial urinary sphincter placement for incontinence in high-risk patients after treatment of prostate cancer. Urology. 2008 Oct;72(4):825-7. doi: 10.1016/j.urology.2008.06.065. Epub 2008 Aug 26. — View Citation

Dalkin BL, Wessells H, Cui H. A national survey of urinary and health related quality of life outcomes in men with an artificial urinary sphincter for post-radical prostatectomy incontinence. J Urol. 2003 Jan;169(1):237-9. — View Citation

Guralnick ML, Miller E, Toh KL, Webster GD. Transcorporal artificial urinary sphincter cuff placement in cases requiring revision for erosion and urethral atrophy. J Urol. 2002 May;167(5):2075-8; discussion 2079. — View Citation

Haab F, Trockman BA, Zimmern PE, Leach GE. Quality of life and continence assessment of the artificial urinary sphincter in men with minimum 3.5 years of followup. J Urol. 1997 Aug;158(2):435-9. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Revision or removal surgery for AUS cuff problems other than mechanical failure: these include cuff erosion, impending erosion (discretion of surgeon), persistent retention due to small cuff, urethral atrophy		Through study completion, an average of up to 1 year
Secondary	Rate of post-operative urinary retention	Urinary retention defined as urinary catheter placement for more than 5 days post-op.	Up to 2-4 weeks
Secondary	Change in 24 hour pad test at 3 months post-op compared to pre-op		3 months post op
Secondary	Erectile function as measured pre and post AUS placement via the Sexual Health Inventory for Men (SHIM)	Sexual health is an important part of an individual's overall physical and emotional well being. This questionnaire is designed to help identify if the patient may be experiencing erectile dysfunction.	3 month post op, 12 month post op
Secondary	Incontinence impact as measured by the Incontinence Symptom Index (ISI)	This brief questionnaire is designed to assess the severity of the patient's urinary incontinence	3 month post op, 12 month post op
Secondary	Quality of Life impact as measured by the Incontinence Impact Questionnaire--Short Form (IIQ)	Some people find that accidental urine loss may affect their activities, relationships, and feelings. The questions in this assessment refer to areas in the subjects life that may have been influenced or changed by incontinent symptoms.	3 month post op, 12 month post op