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Neurogenic Incontinence clinical trials

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NCT ID: NCT01465581 Terminated - Clinical trials for Dysfunctional Voiding

Treatment of Neurogenic Incontinence by Surgery to Cut the Filum Terminale

NICNOC
Start date: July 2011
Phase: N/A
Study type: Observational

The target population of this study is children with primary or secondary daytime urinary incontinence, who have failed to improve adequately despite compliance with at least 6 months of standard medical therapy. The study hypothesis is that patients who under go cutting the filum terminale - the string-like lower end of the spinal cord - will have improved bladder function at 6-month follow up. Bladder function and its effects on quality of life will be measured before surgery and at 6-month follow up.