Enuresis Alarm - Is a Manual Trigger System Beneficial?

  • STATUS
    Recruiting
  • End date
    Sep 12, 2023
  • participants needed
    200
  • sponsor
    Gina Lockwood
Updated on 3 March 2022

Summary

The purpose of this study is to evaluate whether the bedwetting alarm trigger activated by parents to wake their child, in addition to the moisture alarm, will improve treatment success compared to the moisture alarm alone.

Description

Nocturnal enuresis is a common issue in children, and use of bedwetting alarms has shown the best long-term success. However, use of alarms is very time-intensive, often taking months before yielding results. Researchers in the division of pediatric urology are initiating a randomized controlled study comparing a standard bedwetting alarm with a newly developed technology, with the hope that the new alarm will result in better, more rapid, and easier treatment for bedwetting.

Children between the ages of 5 to 15 years old who have issues with bedwetting after successful toilet training may qualify for the study.

Participants must first be evaluated by a pediatric urology specialist.

Details
Condition Enuresis, Nocturnal
Treatment Manual Trigger, Normal, Normal
Clinical Study IdentifierNCT03522818
SponsorGina Lockwood
Last Modified on3 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

children ages 5-15 years
Diagnosis of Primary Monosymptomatic Nocturnal Enuresis
>2 wet nights per week
Score of 7 or below on questions 1-6 and 9-13 on Vancouver Dysfunctional Elimination Questionnaire
Patients/parents compliance in recording data > 50% of nights

Exclusion Criteria

Known comorbid conditions: daytime incontinence, anatomic abnormalities (hydronephrosis, VUR), recurrent urinary tract infection, dysuria, neurogenic bladder, developmental delay, encopresis, diabetes insipidus, previous history of urologic surgery
Concomitant DDAVP use, anticholinergic use, B3 agonist use
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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