BOTOX® Intravesical Instillation in Participants With Overactive Bladder and Urinary Incontinence
| Status: | Recruiting |
|---|---|
| Conditions: | Overactive Bladder, Urology |
| Therapuetic Areas: | Gastroenterology, Nephrology / Urology |
| Healthy: | No |
| Age Range: | 18 - 75 |
| Updated: | 4/17/2018 |
| Start Date: | October 4, 2017 |
| End Date: | March 3, 2020 |
| Contact: | Clinical Trials Registry Team |
| Email: | IR-CTRegistration@allergan.com |
| Phone: | 877‐277‐8566 |
A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Single-treatment, 2-stage, Dose-finding Study Evaluating the Efficacy and Safety of BOTOX® Intravesical Instillation in Participants With Overactive Bladder and Urinary Incontinence
This study will evaluate the efficacy and safety of BOTOX® intravesical instillation in
participants with overactive bladder and urinary incontinence.
participants with overactive bladder and urinary incontinence.
Inclusion Criteria:
- Symptoms of OAB (frequency/urgency) with urinary incontinence for at least 6 months
- Inadequate response or limiting side effects with pharmacotherapy for the treatment of
OAB
Exclusion Criteria:
- Overactive Bladder caused by neurological condition
- Patient has predominance of stress incontinence
- History or evidence of pelvic or urological abnormality
- Prior use of BOTOX for any urological condition
We found this trial at
23
sites
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University of Pittsburgh The University of Pittsburgh is a state-related research university, founded as the...
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1579 Straits Turnpike
Middlebury, Connecticut 06762
Middlebury, Connecticut 06762
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Virginia Mason Medical Center Established in 1920, Virginia Mason began as an 80-bed hospital with...
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