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NCT00190814 · ClinicalTrials.gov registry record · Phase 3
Effectiveness and Safety of Duloxetine in Women Experiencing Urinary Leakage Due to Physical Stress and Urge.
A Phase 3 study, sponsored by Eli Lilly and Company.
- Completed
- Registry status
- Phase 3
- Development phase
- 600
- Enrollment target
NCT00190814: Completed Phase 3 study, sponsored by Eli Lilly and Company.
NCT00190814 is a Phase 3 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 600 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (22% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00190814, a Phase 3 study, has completed, sponsored by Eli Lilly and Company.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 600 participants
- Enrollment target
Study Summary
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.
Interventions
- DRUG placebo
- DRUG duloxetine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 2003-09 |
| Est. Completion | 2006-05 |
| Phase | Phase 3 |
What the finished NCT00190814 record still lists
NCT00190814 is an interventional study that assigns participants to a tested intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (22% lower).
The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.
NCT00190814 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00190814 about?
NCT00190814 is a clinical study titled "Effectiveness and Safety of Duloxetine in Women Experiencing Urinary Leakage Due to Physical Stress and Urge.". 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.
What is the current status of trial NCT00190814?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 600 participants. The study started on 2003-09. Estimated completion is 2006-05.
What interventions are being tested in trial NCT00190814?
The interventions under investigation include: placebo (DRUG), duloxetine (DRUG).
Who is sponsoring clinical trial NCT00190814?
This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00190814's enrollment target sits among peer trials
600 608th of 2000 higher than 1,363 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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