Treatment of Persistent Urinary Incontinence in Children

NCT00124046 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2016-06-01

No results posted yet for this study

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.

Conditions

Interventions

PROCEDURE

Surgery

Surgery for this diagnosis is a standard of care, as is the medical treatment. We are comparing the two

PROCEDURE

Medical Treatment

Surgery for this diagnosis is a standard of care, as is the medical treatment. We are comparing the two

Sponsors & Collaborators

  • Vancouver Foundation

    collaborator OTHER
  • University of British Columbia

    lead OTHER

Principal Investigators

  • Paul Steinbok, MB, BS, FRCSC · Children's and Women's Health Centre of British Columbia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
5 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-30
Primary Completion
2014-12-31
Completion
2015-10-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00124046 on ClinicalTrials.gov