Expired Study
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Nashville, Tennessee 37232


Purpose:

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.


Study summary:

Subjects with non-neurogenic over-active bladder and urge predominant incontinence who are intolerant to medical therapy or have persistence of symptoms despite medical therapy and require augmentation cystoplasty 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.


Criteria:

Inclusion Criteria: - 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 Exclusion Criteria: - 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


NCT ID:

NCT00594139


Primary Contact:

Study Director
Michael Tillinger, MD
Tengion, Inc


Backup Contact:

N/A


Location Contact:

Nashville, Tennessee 37232
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 17, 2018

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