Skip to main content
OpenTrials
Completed

NCT Number: NCT00244296

To Determine How Effective Duloxetine is in Treating Women 65 Years and Older With Symptoms of Stress Urinary Incontinence, or With a Combination of Stress Urinary Incontinence and Urge Urinary Incontinence Symptoms

The purpose of this study is to determine how effective duloxetine is in treating women who are 65 years of age or older with symptoms of stress urinary incontinence, or with a combination of stress urinary incontinence and urge urinary incontinence symptoms.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Urinary Incontinence, Stress Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Lower Urinary Tract Symptoms Male Urogenital Diseases Pathological Conditions, Signs and Symptoms Signs and Symptoms Urinary Incontinence Urination Disorders Urogenital Diseases Urologic Diseases Urological Manifestations

Age range

65 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Champcueil, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • female outpatient greater than or equal to 65 years of age
  • have symptoms of SUI or stress-predominant MUI for at least 3 consecutive months
  • have at least 7 incontinence episodes per week. For patients with MUI, at least 50% of the IEF must be due to stress.
  • is ambulatory and able to use a toilet independently and without difficulty

Exclusion criteria

  • at Visit 1 have a positive urine culture or a history of four or more urinary tract infections (UTIs) in the preceding year
  • have had continence surgery or received bladder neck bulking agent therapy within 3 months prior to study entry
  • began pelvic floor muscle exercises (for example, Kegel or biofeedback) within 3 months prior to study entry or at any time during the study.
  • have neurologic lesions or conditions (e.g. multiple sclerosis, spinal cord lesions or Parkinson's disease) or local lesions (e.g. bladder stones present or tumors) that affect the lower urinary tract.
  • intake of monoamine oxidase inhibitors (MAOIs) within 14 days prior to randomisation or at any time during the study

Treatment and study plan

duloxetine hydrochloride

Drug

Placebo

Drug

Primary outcomes

  1. Assess the efficacy of duloxetine for up to 12 weeks, compared to placebo, in community dwelling women > or = 65 years of age with symptoms of pure stress urinary incontinence (SUI) or stress-predominant mixed urinary incontinence

Secondary outcomes

  1. Compare the efficacy of duloxetine 40 mg twice daily with that of placebo in the treatment of the symptoms of SUI and stress-predominant MUI as measured by:Absolute change in IEF

  2. Change in mean time between voids

  3. Percent change in the number of continence pads used per week

  4. Change in the Incontinence Quality of Life total score and 3 sub-domain scores

  5. Responder analysis based on the established within-treatment minimal clinically important difference established for the I-QOL

  6. Responder analysis based on percent change in IEF

  7. Patient's rating of improvement using the PGI-I

  8. Compare efficacy of duloxetine 40 mg twice daily with that of placebo as measured by the percent change in IEF using in the SUI and MUI subgroups

  9. To assess the impact of treatment with duloxetine 40 mg twice daily and placebo on the development of suicidal ideation.

  10. Assess the impact of treatment with duloxetine 40 mg twice daily and placebo in cognition.

  11. Assess the impact of treatment with duloxetine 40 mg twice daily and placebo as measured by changes in BDI-II.

  12. To compare the safety of duloxetine with placebo based on changes in vital signs, clinical lab values, occurrence and duration of adverse events and premature discontinuation of study due to adverse events.

Sponsors and collaborators

Lead sponsor

Eli Lilly and Company

Industry

Collaborators

  • Boehringer Ingelheim

Registry information

Official study title

A Double-Blind, Stratified, Randomised, Parallel, Placebo-Controlled, Multi-Centre Study to Assess the Efficacy and Safety of Duloxetine (20 mg Bid for 2 Weeks Escalating to 40 mg Bid) for up to 12 Weeks, Compared to Placebo, in Community-Dwelling Elderly Women > or = 65 Years of Age With Symptoms of Stress Urinary Incontinence or Stress-Predominant Mixed Urinary Incontinence.

Important dates

Study start
2005
Study completion
2007
First posted
Oct 26, 2005
Registry last updated
Jan 26, 2007

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.

Related clinical trials

Published trials that share one or more normalized conditions with this study.