Anatomical and Functional Differences Between Continent and Incontinent Men Post Radical Prostatectomy

Sponsor
University of Michigan (Other)
Overall Status
Terminated
CT.gov ID
NCT01832831
Collaborator
(none)
24
2
55
12
0.2

Study Details

Study Description

Brief Summary

One out of every six men will be diagnosed with prostate cancer and post prostatectomy up to 75% report urinary incontinence. There are many hypotheses about the exact cause of post prostatectomy stress incontinence (PPI). Existing studies have focused on surgical or cadaveric dissections to define structures responsible for PPI. Contemporary 3T MRI now allows three dimensional, sub-millimeter resolution of the human pelvis and clearly demonstrates pelvic anatomy without the distortion of dissection. It is our overarching hypothesis that PPI is multifactorial and occurs because of a combination of specific anatomical and functional impairments. We propose conducting a case control study with matching for age and race to compare the MRI anatomy and urinary tract function on urodynamics between 20 men with PPI (cases) and 20 men who are continent post prostatectomy (controls) who are all a minimum of 12 months post surgery. We will use static and dynamic MRI at 3 Tesla to make objective measurements of the bladder neck, external urethral sphincter, pelvic floor, urethral anastomotic fibrosis, and urethral hypermobility- all believed to play a large part in continence. Multi-channel urodynamic studies will also be performed to assess the leak point and maximum urethral closure pressure. All cases and controls will complete standardized questionnaires - the AUA symptom index and the Incontinence Severity Index as a quality of life measure. This study is needed to provide critical information about causes of male PPI, a quality of life altering voiding dysfunction, and will assist with the advancement of pharmacological and surgical treatment of this disease.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    24 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Study Start Date :
    May 1, 2010
    Actual Primary Completion Date :
    Feb 1, 2013
    Actual Study Completion Date :
    Dec 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Continent Men

    Incontinent Men

    Outcome Measures

    Primary Outcome Measures

    1. Thickness and length of both the smooth muscle and striated muscle external urethral sphincter [2 years]

      Structural assessment

    2. Posterior urethral length from the bladder neck to the perineal membrane. [2 years]

      Structural assessment

    3. Levator ani thickness [3 years]

      Structural assessment

    4. Thickness and length of anastomotic fibrosis in both sagittal and axial planes [3 years]

      Structural assessment

    5. Maximal urethral closure pressure [3 years]

      Functional assessment

    6. Increase in urethral pressure during maximal muscle contraction [3 years]

      Functional assessment

    7. Urethral hypermobility on MRI [3 years]

      Functional assessment

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    21 Years and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Only men will be included since this is a study of post prostatectomy incontinence. Cases will be comprised of men who are post radical retropubic or laparoscopic (robotic) prostatectomy who have stress urinary incontinence based on history and a minimum of 50 grams of urine loss on 24 hour pad weights. Controls will be comprised of men who are post radical retropubic or laparoscopic (robotic) prostatectomy who do not have any kind or amount of incontinence based on history. Cases and controls will be matched for both age and race these have been shown to alter anatomical appearance of structures and lower urinary tract function.
    Exclusion Criteria:
    • Criteria for both groups include urge incontinence, urinary retention, neurologic disease, insulin dependent diabetes, high dose steroid use, pre-surgical abnormal voiding function or incontinence, prior pelvic radiation or urologic surgery, any prior incontinence surgery, current medical therapy for incontinence or a perineal route of radical prostatectomy since this had been shown to give a distinctly different appearance on MRI compared to the laparoscopic or retropubic approach. Any patient with pelvic or systemic recurrence of their prostate cancer will also be excluded. Any man with relative or absolute contraindications to MRI such as implants or claustrophobia will be excluded.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 VA Ann Arbor Healthcare System Ann Arbor Michigan United States 48105
    2 University of Michigan Ann Arbor Michigan United States 48109

    Sponsors and Collaborators

    • University of Michigan

    Investigators

    • Principal Investigator: Anne Pelletier-Cameron, MD, University of Michigan

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Anne Pelletier-Cameron, Associate Professor, Urology, University of Michigan
    ClinicalTrials.gov Identifier:
    NCT01832831
    Other Study ID Numbers:
    • HUM00035833
    First Posted:
    Apr 16, 2013
    Last Update Posted:
    Apr 21, 2016
    Last Verified:
    Apr 1, 2016
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 21, 2016