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Completed

NCT Number: NCT00212264

Conservative Treatment of Postprostatectomy Incontinence

The primary purpose of this study is to test the effectiveness, impact on quality of life, and durability of non-surgical therapies for incontinence persisting at least one year after surgery. The study is a a prospective, controlled, randomized trial comparing an 8-week, multi-component behavioral training program (pelvic floor muscle exercises, self-monitoring with bladder diaries, regular office visits, bladder control techniques, and fluid management) to the same program with the addition of biofeedback and pelvic muscle electrical stimulation.

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Key information

About this study

The primary purpose of this project is to test the effectiveness, impact on quality of life, and durability of conservative therapies for persistent post-prostatectomy urinary incontinence in a prospective, controlled, randomized trial comparing an 8-week, multi-component behavioral training program (pelvic floor muscle exercises, self-monitoring with bladder diaries, regular office visits, bladder control techniques, and fluid management) to the same program with the addition of biofeedback and pelvic muscle electrical stimulation.

The second purpose of the study is to examine and compare the cost-effectiveness of the 8-week, multi-component behavioral training program to the same program with the addition of biofeedback and pelvic floor electrical stimulation.

Prostate cancer is the most common internal cancer in men in the United States. The most common treatment for early disease is radical prostatectomy, the removal of the prostate gland. The two most common sequelae of prostatectomy are incontinence and erectile dysfunction. The incontinence improves and often resolves in the first year after prostatectomy, but surveys of patients show that 40% of men have incontinence severe enough to require pads 1 and 2 years after their surgery. There are currently no randomized, controlled studies of non-surgical treatments for persistent post-prostatectomy incontinence.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Involuntary loss of urine that started immediately after radical prostatectomy and has persisted for at least one year.
  • One-week bladder diary with interpretable data and at least two incontinence episodes

Exclusion criteria

  • Any unstable medical condition, particularly decompensated congestive heart failure, history of malignant arrhythmias, or unstable angina
  • Cardiac pacemaker or implanted cardiac defibrillator
  • Current use of anticholinergic agents for detrusor instability
  • Folstein's Mini-Mental State Exam score below 24 (impaired mental status)
  • One-week bladder diary with continual leakage - defined as always being damp or wet or unable to quantitate individual accidents.
  • Poorly controlled diabetes, defined as (glycosylated hemoglobin > 9 within last 3 months).
  • Hematuria on microscopic examination. Enrollment will be permitted after urologic evaluation.
  • Urodynamic evaluation: Post-void residual volume greater than 200 mL

Treatment and study plan

Behavioral therapy

Behavioral

Pelvic Floor Muscle Exercises and Bladder control strategies

Pelvic Floor Electrical Stimulation

Device

Pelvic Floor Electrical Stimulation daily for 8 weeks

Biofeedback

Behavioral

Pelvic Floor Muscle training via biofeedback

No treatment

Other

No treatment

Primary outcomes

  1. Percent Change in Incontinence Episodes on Bladder Diary

    Time frame: 2 months

    [(Baseline incontinence episodes minus 2-month incontinence episodes)/baseline incontinence episodes] x 100%

  2. Percent Change in Incontinence Episodes Per Week on Bladder Diary

    Time frame: 1 year

    [(Baseline incontinence episodes minus 12-month incontinence episodes)/baseline incontinence episodes] x 100%

Sponsors and collaborators

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Nih

Registry information

Important dates

Study start
2003
Primary completion
2008
Study completion
2011
First posted
Sep 21, 2005
Registry last updated
Apr 11, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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