Expired Study
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Wilmington, Delaware 19803


Purpose:

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.


Criteria:

Inclusion Criteria: - Primary or secondary daytime urinary incontinence, persistent over at least 6 months of medical treatment. - Abnormal urodynamic testing - Normal conus on magnetic resonance imaging of the spine - Dysfunctional Voiding Symptom Scale score greater than 6 for girls or greater than 9 for boys Exclusion Criteria: - Bladder outlet obstruction - Bladder atony - Congenital anorectal malformation - Additional diagnoses independently associated with neurogenic bladder dysfunction - Encephalopathy precluding reasonable expectation of attainment of continence - Inability to comply with medical management - Unwillingness to comply with initial or follow up urodynamic testing


NCT ID:

NCT01465581


Primary Contact:

Principal Investigator
Joseph H Piatt, MD
Alfred I. duPont Hospital for Children


Backup Contact:

N/A


Location Contact:

Wilmington, Delaware 19803
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 21, 2017

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