Skip to main content
OpenTrials
Completed

NCT Number: NCT00148005

Prevalence, Etiology and Therapy of Micturition Disorders of Children With a Mental and/or Motoric Disability

Investigation of the prevalence etiology and therapy of micturition disorders of children with a mental and/or motoric disability

Completed

Looking for future studies?

Notify Me

Key information

Age range

4 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Ghent

Ghent, 9000, Belgium

About this study

Overview of the problem by a questionnaire, diary of micturition and drinking behaviour, filled out by the parents or by the staff of the institution.

Investigation of the etiology by clinical and functional examination (uroflowmetry, bladder scan, video-urodynamic examination).

Frequency:

  • Uroflowmetry: two periods of two weeks, with 6 weeks break between both periods. During the follow-up period every 3 months during 12 months
  • Bladder scan: once during the periods of the uroflowmetry
  • Video-urodynamic examination: once in selected participants, after consent of the parents
  • Adaptation of the drinking behaviour: start after two weeks of observation, after uroflowmetry and bladder scan. Continuous proces.
  • Therapeutic measures (medication, miction clock): start after 10 weeks of observation or after video-urodynamic examination.

Development of a therapeutic plan: adaptation of the micturition and drinking behaviour, anticholinergic therapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children with a motoric and/or mental disability
  • 4-14 years

Exclusion criteria

  • Known neurogenic bladder disorder

Treatment and study plan

Questionnaire and micturition and drinking diaries

Procedure

Clinical and functional examination (uroflowmetry, bladder scan and video-urodynamic examination)

Procedure

Adaptation of the drinking scheme

Behavioral

Anticholinergic therapy

Drug

Micturition clock

Behavioral

Primary outcomes

  1. Prevalence of micturition disorders

  2. Etiology of micturition disorders after 10 weeks observation

  3. Influence of drinking scheme on bladder capacity and micturition continence after 10 weeks observation

Secondary outcomes

  1. Efficacy of the therapy after 3, 6, 9, 12 months

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Registry information

Important dates

Study start
2004
First posted
Sep 7, 2005
Registry last updated
Dec 28, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.