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Treatment of Persistent Urinary Incontinence in Children

Primary Purpose

Urinary Incontinence

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Surgery
Medical Treatment
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Incontinence focused on measuring Urinary Incontinence in Children, Surgical Section of the Filum Terminale, Occult Tethered Cord Syndrome, Urodynamic Scale, Enuresis-Specific Quality of Life Scale

Eligibility Criteria

5 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Urologic Inclusion Criteria: Primary or secondary daytime urinary incontinence, persistent over 12 months of medical treatment An abnormal 3 day voiding diary compiled over a 3 week voiding period completed after 12 months of medical treatment Normal bladder ultrasound (if bladder ultrasound shows more than minimal bladder thickening [>3.0mm at 50% filling of expected capacity or less] then a voiding cystourethrogram [VCUG] will be required to rule out bladder outlet obstruction) Abnormal urodynamic testing Radiologic Inclusion Criteria: Normal position conus medullaris Any size filum terminale Any amount of fat in the filum terminale Terminal syringomyelia of less than one bony level is acceptable Lumbar bifid spinal lamina is acceptable Exclusion Criteria: Patients with evidence of significant, progressive, lower extremity motor or sensory deficits, with evidence of progression over the previous 6 months The presence of cutaneous markings on the back, in the absence of confirmatory magnetic resonance imaging (MRI) findings of a specific spinal dysraphism does not exclude the patient from participation

Sites / Locations

  • Children's and Women's Health Centre of British Columbia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Surgical

Medical Treatment

Arm Description

Outcomes

Primary Outcome Measures

Quality of life, as measured by a validated enuresis-specific quality of life scale

Secondary Outcome Measures

Any of the following radiographic findings leads to improved response to section of the filum: fat in the filum terminale, thickened filum terminale, presence of bifid lamina
Presence of a growth spurt in the 6 months following the section of the filum compared to the 6 months prior
Duration of urinary symptoms is negatively associated with improvement in urinary function
The following subtle neurological abnormalities are predictors of good outcome following filum section: strength or sensory dysfunction, clinical symptoms of back or leg pain, inability to touch toes with forward flexion
Section of the filum terminale leads to reduced frequency of urinary infections in the 12 months following surgery

Full Information

First Posted
July 22, 2005
Last Updated
May 30, 2016
Sponsor
University of British Columbia
Collaborators
Vancouver Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00124046
Brief Title
Treatment of Persistent Urinary Incontinence in Children
Official Title
Treatment of Persistent Urinary Incontinence in Children
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia
Collaborators
Vancouver Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether surgical section of the filum terminale in children, when added to standard medical therapy, will result in a reliable and clinically-significant improvement in two main markers of incontinence within/at 12 months after treatment.
Detailed Description
Eight % to sixteen % of school-aged children or approximately 50,000 children in British Columbia (BC) suffer from persistent urinary incontinence (i.e., beyond age 5 years, when continence is usually achieved). Prevalence decreases with age, yet studies indicate that 10%-25% of healthy adolescents and young adults also suffer from incontinence. Persistent incontinence has profound social, emotional and behavioral impacts, and adversely affects the quality of life of affected children and their families. Typical management of incontinence in these patients includes repeated visits to the family doctor and long-term lifestyle changes and/or prescription use. Each year in BC, family doctors refer about 4500 children to pediatric urologists at BC Children's Hospital (BCCH). BCCH is the only tertiary care facility for children and youth in the province, so that children and parents come from all over BC for these appointments and for diagnostic urodynamics testing. Of these children who are evaluated by pediatric urologists each year, approximately 900 (20%) are designated as having dysfunctional voiding. In this group, following one year of non-responsiveness to medical treatment (medication, lifestyle), the urologist may refer the child to neurosurgery for assessment and possible surgery. In recent years, the referral rate of children with incontinence to BCCH Neurosurgery has increased markedly from 1-2 to 12-15 children per year. This referral is because urinary incontinence in children is one of the clinical features of a tethered cord syndrome. In this syndrome, the lower end of the spinal cord (the conus) is pulled down lower than normal by a thickened band of tissue called the filum terminale, which runs inferiorly from the bottom of the spinal cord. This "tethered" condition can be treated by surgical section of the filum terminale. More recently, the concept of an occult tethered cord syndrome (OTCS) has been proposed; in OTCS, clinical symptoms (e.g., incontinence) are consistent with a tethered cord syndrome, but the conus ends at a normal location. The concept of the OTCS is controversial, and it is not yet clear whether or not section of the filum is appropriate. Filum section is a relatively minor procedure (akin to appendectomy) that requires general anesthesia during day surgery. In uncontrolled case series, section of the filum terminale in children with OTCS resulted in a 60%-97% improvement in symptoms. Given this evidence that section of the filum may improve incontinence symptoms, urologists are keen to refer more patients to neurosurgeons. Furthermore, families are demanding more tests and options, and are ready to pursue surgery as treatment of their child's incontinence. This suggests that the referral rate to Neurosurgery will continue to increase, and there will be a crucial requirement to develop standard policies and procedures related to offering this surgery to children with incontinence. As yet, however, the effectiveness and appropriateness of the surgery have not been evaluated systematically. To investigate this matter a comparison will be made between two randomized groups. One group will undergo early tethered cord release by section of the filum terminale through a limited posterior lumbar spinal exposure and continued medical therapy for 12 months. This group will be compared to a second that has continued standard medical therapy without surgical intervention for a further 12 months. This comparison will be made based on physiological markers of urinary incontinence, as measured by a urodynamic scale; and quality of life, as measured by a validated enuresis-specific quality of life scale. The intervention will be considered to be successful if it improves the urodynamic score by 20%, and the quality of life of the child and his family are significantly improved.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence
Keywords
Urinary Incontinence in Children, Surgical Section of the Filum Terminale, Occult Tethered Cord Syndrome, Urodynamic Scale, Enuresis-Specific Quality of Life Scale

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgical
Arm Type
Active Comparator
Arm Title
Medical Treatment
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Surgery
Intervention Description
Surgery for this diagnosis is a standard of care, as is the medical treatment. We are comparing the two
Intervention Type
Procedure
Intervention Name(s)
Medical Treatment
Intervention Description
Surgery for this diagnosis is a standard of care, as is the medical treatment. We are comparing the two
Primary Outcome Measure Information:
Title
Quality of life, as measured by a validated enuresis-specific quality of life scale
Secondary Outcome Measure Information:
Title
Any of the following radiographic findings leads to improved response to section of the filum: fat in the filum terminale, thickened filum terminale, presence of bifid lamina
Title
Presence of a growth spurt in the 6 months following the section of the filum compared to the 6 months prior
Title
Duration of urinary symptoms is negatively associated with improvement in urinary function
Title
The following subtle neurological abnormalities are predictors of good outcome following filum section: strength or sensory dysfunction, clinical symptoms of back or leg pain, inability to touch toes with forward flexion
Title
Section of the filum terminale leads to reduced frequency of urinary infections in the 12 months following surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Urologic Inclusion Criteria: Primary or secondary daytime urinary incontinence, persistent over 12 months of medical treatment An abnormal 3 day voiding diary compiled over a 3 week voiding period completed after 12 months of medical treatment Normal bladder ultrasound (if bladder ultrasound shows more than minimal bladder thickening [>3.0mm at 50% filling of expected capacity or less] then a voiding cystourethrogram [VCUG] will be required to rule out bladder outlet obstruction) Abnormal urodynamic testing Radiologic Inclusion Criteria: Normal position conus medullaris Any size filum terminale Any amount of fat in the filum terminale Terminal syringomyelia of less than one bony level is acceptable Lumbar bifid spinal lamina is acceptable Exclusion Criteria: Patients with evidence of significant, progressive, lower extremity motor or sensory deficits, with evidence of progression over the previous 6 months The presence of cutaneous markings on the back, in the absence of confirmatory magnetic resonance imaging (MRI) findings of a specific spinal dysraphism does not exclude the patient from participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Steinbok, MB, BS, FRCSC
Organizational Affiliation
Children's and Women's Health Centre of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's and Women's Health Centre of British Columbia
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6H 3V4
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
26926544
Citation
Steinbok P, MacNeily AE, Hengel AR, Afshar K, Landgraf JM, Hader W, Pugh J. Filum Section for Urinary Incontinence in Children with Occult Tethered Cord Syndrome: A Randomized, Controlled Pilot Study. J Urol. 2016 Apr;195(4 Pt 2):1183-8. doi: 10.1016/j.juro.2015.09.082. Epub 2016 Feb 28.
Results Reference
derived

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Treatment of Persistent Urinary Incontinence in Children

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