Expired Study
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Baltimore, Maryland 21204


Purpose:

The purpose of the study is to evaluate the effectiveness of duloxetine in reducing urinary incontinence(leakage of urine)occurrences in women due to physical stress and leakage that occurs during a strong need(urge) to urinate.


Criteria:

Inclusion Criteria: - female outpatients greater than or equal to 18 years of age. - experience episodes of urinary incontinence based on diagnostic criteria of at least 4 episodes a week with symptoms for a minimum of three months prior to start of study. - have an educational level and degree of understanding English. - are free of urinary tract infections. - have a discreet episodes of incontinence(i.e. dry between episodes and do not continuously leak.) Exclusion Criteria: - have received treatment for incontinence within the last 5 years. - suffer from severe constipation. - currently nursing or breast feeding. - any nervous system disease that would affect normal urinary function. - any extension of internal organs beyond the vaginal opening.


NCT ID:

NCT00190814


Primary Contact:

Study Director
Call 1-877-CTLILLY (1-877-285-4559 or 1-317-615-4559) Monday-Friday 9am-5pm Eastern time (UTC/GMT - 5 hours, EST)
Eli Lilly and Company


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland 21204
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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