Autologous Neo-Bladder Construct in Non-Neurogenic Overactive Bladder and Urge Predominant Incontinence
Withdrawn before enrolling · Phase 2
Conditions studied: Overactive Bladder
In brief
Subjects with non-neurogenic over-active bladder will be enrolled. The hypothesis is that augmentation cystoplasty using an autologous neo-bladder construct will increase functional capacity and thereby reduce the number of micturition episodes per day in subjects with non-neurogenic over active bladder and urge predominant incontinence.
Key facts
- Study ID
- NCT00594139
- Run by
- Tengion
- People needed
- 0
- Starts
- 2008-01-01
- Expected to finish
- 2008-01-01
- Last updated by the study team
- 2018-06-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- History of non-neurogenic overactive bladder for at least 12 months prior to study entry
- Intolerance to medical therapy or persistence of symptoms despite medical therapy
You may not qualify if…
- Subjects with stress incontinence or mixed incontinence where the predominant component is stress incontinence
- Use of Botulinum Toxin A injections into the bladder within the previous 6 months
- Presence of a neuromodulator
- Using catheterization as a way to control incontinence
- History of bladder cancer
Where it is running
- Vanderbilt University — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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