Biomechanical Effects of Duloxetine on Bladder and Sphincter Muscle Function in Women in Pure Genuine Stress Incontinence

Completed · Phase 2 · Has a placebo group

Conditions studied: Urinary Stress Incontinence

In brief

Double-blind placebo-controlled study of the biomechanical effects of duloxetine compared with placebo in the treatment of women with pure genuine stress incontinence

Key facts

Study ID

NCT00190567

Run by

Eli Lilly and Company

People needed

50

Starts

2001-10-01

Expected to finish

2006-04-01

Last updated by the study team

2007-01-26

Who can join

Age: 18 and older, up to 75. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female
• Between 18 and 75 years of age
• Diagnosis of GSI
• Have discrete episodes of incontinence

You may not qualify if…

• Positive urine culture at visit 1
• Use of MAOI
• Have had continence or urethral surgery
• Use of anti-incontinence device, vaginal pessaries or medications for the treatment of urinary incontinence
• Began pelvic floor muscle exercises within 6 months prior to study entry.

Where it is running

• For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday - Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5hours, EST), or speak with your personal physician — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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