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OpenTrials
Completed

NCT Number: NCT00178191

Randomized Trial for Botox Urinary Incontinence

The purpose of this study is to determine how effective Botox is in reducing the amount of urine leaked and which dose of Botox is more effective and safe in those who have urinary urge incontinence.

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Key information

Age range

21 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Rochester

Rochester, New York, 14642, United States

About this study

The prevalence of urinary incontinence in the US ranges from 3-14% with epidemiologic estimates ranging widely.1 Most urinary incontinence can be categorized into stress urinary incontinence (SUI) or UUI with UUI remaining more common and debilitating than SUI.2 A major cause of UUI is overactive bladder or detrusor instability (DI), and while DI is very common, its etiology remains unknown. DI is often successfully managed with behavioral therapy, physical therapy, medications and surgery with the most effective therapy being anticholinergic medication.2 However, side effects including dry mouth, and constipation often lead to discontinuation of these drugs. In addition, many patients fail anticholinergic medication and have persistent urinary leakage. Women who fail these treatments have limited options.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Subjects must have ALL of the following:

  • Completed a routine evaluation of incontinence (urodynamics, bladder diaries, and pad weights) through the urogynecology clinic at SMH within 3 months of the screening visit
  • Symptoms of urge incontinence associated with leakage on bladder diary
  • 24-hour pad weight >100 cc's (volume requiring multiple daily diaper changes)
  • Absence of a bladder infection or other condition that could explain urinary leakage
  • Absence of stress incontinence or a cough leak point pressure > 100 cm H2O on cystometry (this correlates with mild stress incontinence)
  • Failed anticholinergic therapy
  • Willingness and ability to perform intermittent clean catheterization (due to the risk of prolonged urinary retention from Botox)
  • The ability and willingness to return for surveillance evaluations
  • A negative urine pregnancy test if at risk for pregnancy
  • Competent to give signed consent and complete all of the study measures

Exclusion criteria

  • Children (< 21 years old), pregnant women and prisoners
  • History of carcinoma of the bladder
  • Absence of a measurable detrusor contraction on a pressure flow micturition study
  • A foreign body in the bladder or other correctable etiology for the UUI
  • Prior documented resistance to Botox
  • Gross fecal incontinence (due to confounding effects on pad weights and counts)
  • Known allergy to lidocaine or related compounds (used for local analgesia)
  • Known allergy to or inability to take both Bactrim DS or Ciprofloxacin (used for urinary tract infection prophylaxis)
  • Current use of an aminoglycoside or preparing for general anesthesia within 1 week (risk of synergetic effects
  • Known neurologic conditions such as Parkinson's disease, myasthenia gravis, multiple sclerosis, autonomic dysfunction, Lambert-Eaton syndrome, Amyotrophic Lateral Sclerosis or other neurologic disorder that may impact urinary function or the effect of Botox.

Treatment and study plan

Bladder diary

Other

3-day bladder diary

questionnaires

Other

Incontinence Quality of Life questionnaires

Urodynamics

Procedure

Urodynamics

Pad weight

Other

Pad weight

Primary outcomes

  1. Episodes/Day

    Time frame: 9 months

    number of incontinence episodes/day

Sponsors and collaborators

Lead sponsor

University of Rochester

Other

Collaborators

  • National Institute on Aging (NIA)
  • National Institutes of Health (NIH)

Registry information

Official study title

A Randomized Trial of Botox for Severe Urge Incontinence

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
Sep 15, 2005
Registry last updated
Oct 3, 2011

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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