Duloxetine in the Treatment of Stress Urinary Incontinence.
NCT ID: NCT00191087
Last Updated: 2007-01-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
458 participants
INTERVENTIONAL
2001-04-30
2006-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Duloxetine
Eligibility Criteria
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Inclusion Criteria
* 7 or more incontinence episodes per week.
Exclusion Criteria
18 Years
75 Years
FEMALE
No
Sponsors
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Boehringer Ingelheim
INDUSTRY
Eli Lilly and Company
INDUSTRY
Principal Investigators
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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon-Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Role: STUDY_DIRECTOR
Eli Lilly and Company
Locations
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For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon- Fri from 9AM to 5 PM Eastern time (UTC/GMT - 5 hours, EST) or speak with your personal physician.
London, England, United Kingdom
Countries
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Other Identifiers
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F1J-MC-SBAU
Identifier Type: -
Identifier Source: secondary_id
2686
Identifier Type: -
Identifier Source: org_study_id
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