To Evaluate the Safety of Duloxetine in Patients With Stress Urinary Incontinence
Completed · Phase 3
Conditions studied: Stress Urinary Incontinence
In brief
The patients are being followed in this study to determine the safety of taking the medication Duloxetine for a long period of time. The patients participating in this study suffer from Stress Urinary Incontinence.
Key facts
- Study ID
- NCT00190645
- Run by
- Eli Lilly and Company
- People needed
- 600
- Starts
- 2001-02-01
- Expected to finish
- 2006-05-01
- Last updated by the study team
- 2007-01-26
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Successfully completed the protocol for Study F1J-MC-SBAV.
You may not qualify if…
- Treatment with a drug, not including study medication, that has not received regulatory approval at the time of study entry.
- Use of excluded medications within 14 days prior to study entry or at any time during the study.
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) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician — Denver, Colorado, United States
- 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 — Oakville, Ontario, Canada
Full record on ClinicalTrials.gov
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