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NCT00852696 · ClinicalTrials.gov registry record · NA
Over Active Bladder Patients Having Sling Surgery
A NA study, sponsored by Cleveland Clinic Florida.
- Terminated
- Registry status
- NA
- Development phase
- 1
- Enrollment target
NCT00852696: Clinical Trial NA study, sponsored by Cleveland Clinic Florida.
NCT00852696 is a NA study that was terminated before completion, run by Cleveland Clinic Florida. The registered enrollment target is 1 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00852696, a NA study, was terminated before completion, sponsored by Cleveland Clinic Florida.
- TERMINATED
- Registry status
- NA
- Development phase
- 1 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether treatment with anti-muscarinic medications following sub-urethral sling procedures improves overall subjective and objective outcomes in women with mixed incontinence with primary stress symptoms.
Primary Outcome
Women with mixed incontinence with primary stress symptoms undergoing Sub-Urethral Sling Procedures will be randomized to peri-operative placebo or solifenacin. Subjects in the placebo group will take orally once daily for 9 weeks. Subjects in the Solifenacin group will take orally once daily for 9 weeks.
Interventions
- OTHER Placebo
- DRUG Solifenacin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1 participants |
| Start Date | 2008-02 |
| Est. Completion | 2010-02 |
| Phase | NA |
Why NCT00852696 stopped before completion
NCT00852696 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 1 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00852696 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00852696 about?
NCT00852696 is a clinical study titled "Over Active Bladder Patients Having Sling Surgery". The purpose of this study is to determine whether treatment with anti-muscarinic medications following sub-urethral sling procedures improves overall subjective and objective outcomes in women with mixed incontinence with primary stress symptoms.
What is the current status of trial NCT00852696?
This trial is currently terminated. It is a NA study. The enrollment target is 1 participants. The study started on 2008-02. Estimated completion is 2010-02.
What interventions are being tested in trial NCT00852696?
The interventions under investigation include: Placebo (OTHER), Solifenacin (DRUG).
Who is sponsoring clinical trial NCT00852696?
This trial is sponsored by Cleveland Clinic Florida, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00852696's enrollment target sits among peer trials
1 2001st of 2000 the lowest of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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