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Clinical Trials/NCT00803270
NCT00803270
Terminated
Phase 4

Mixed Incontinence: Medical Or Surgical Approach?

Carelon Research10 sites in 1 country27 target enrollmentOctober 2008

Overview

Phase
Phase 4
Intervention
Surgical
Conditions
Urinary Incontinence
Sponsor
Carelon Research
Enrollment
27
Locations
10
Primary Endpoint
Optimal Outcome of Treatment at 6 Months
Status
Terminated
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to compare treatment outcomes for patients with mixed urinary incontinence (MUI) for whom therapy is initiated with surgery to those for whom therapy is initiated with non-surgical treatment. Women who are bothered by symptoms of both stress and urge incontinence will be randomly assigned to initiate treatment with a surgical (surgery for stress incontinence) vs. a non-surgical (drug and behavioral therapy) approach. Follow-up will be a minimum of 12 Months.

Detailed Description

The purpose of this study is to compare treatment outcomes for patients with mixed urinary incontinence (MUI) for whom therapy is initiated with surgery to those for whom therapy is initiated with non-surgical treatment. Women who are bothered by symptoms of both stress and urge incontinence will be randomly assigned to initiate treatment with a surgical (surgery for stress incontinence) vs. a non-surgical (drug and behavioral therapy) approach. Follow-up will be a minimum of 12 Months.

Registry
clinicaltrials.gov
Start Date
October 2008
End Date
March 2009
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Carelon Research
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Mixed UI as evidenced by stress and urge symptoms reported on MESA (either percent of urge-type symptoms ≥ the percent of stress-type symptoms or urge symptom score ≥7 if stress predominant) followed by report of "moderately" or "greatly"/"quite a bit" bothered to questions 2 and 3 of the 6-item Urinary Distress Index (UDI-6) or questions 16 and 17 of the 20-item Pelvic Fl;oor Distress Index (PFDI-20), respectively (See Appendix C)
  • Moderate or severe UI as evidenced by the corresponding response on the Patient Global Impression of Severity (PGI-S)
  • Incontinence symptoms present for at least (3) months\*
  • Bladder capacity \> 200cc (by any method)
  • Urodynamic Stress Incontinence
  • Eligible for both treatment interventions
  • Available to start intervention within 6 weeks
  • Negative urine dipstick (negative result = trace or less for leukocytes \& nitrites)
  • Available for 12 months of follow-up and able to complete study assessments as per clinician judgment
  • Signed consent form

Exclusion Criteria

  • Age \<21 years\*
  • Currently undergoing or recommended to undergo treatment of pelvic organ prolapse
  • Other indicated/planned concomitant surgery
  • Pregnant or has not completed child bearing\*
  • \<12 months post-partum\*†
  • Active malignancy of cervix, uterus, fallopian tube(s) or ovary \> Stage I, or bladder of any Stage
  • Current catheter use
  • Unevaluated hematuria
  • Participation in another trial that may influence the results of this study
  • Patient can be rescreened after respective time interval has been met. †"Partum" is defined as a delivery or other termination that occurs after 20 weeks gestation.

Arms & Interventions

Surgical Treatment

Surgical treatment will consist of the following evidence-based stress incontinence procedures: mid-urethral slings (TVT, TOT, TVT-O), fascial slings, and Burch colposuspension.

Intervention: Surgical

Non Surgical Treatment

The non-surgical treatment will include two components: 1. Pharmacological therapy with any FDA approved overactive bladder (OAB) drug in approved doses; and 2. Behavioral therapy.

Intervention: Non-Surgical Intervention

Outcomes

Primary Outcomes

Optimal Outcome of Treatment at 6 Months

Time Frame: 6 Months

Composite measure defined as "much better" or "very much better" on Patient Global Impression of Improvement (PGI-I) and "normal" or "mild" on Patient Global Impression of Symptoms (PGI-S). PGI-I is a single item: "Circle the one answer that best describes your urinary tract condition now, compared to how it was before your incontinence treatment" with responses ranging from 1= "Very much better" to 7= "Very much worse." The PGI-S is a single item:; "Circle the one number that best describes how your urinary tract condition is now" with responses ranging from 1 = "Normal" to 4 "Severe".

Secondary Outcomes

  • Optimal Outcome of Treatment at 3 Months(3 months)

Study Sites (10)

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