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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00148005
Enrollment
250
Registered
2005-09-07
Start date
2004-09-30
Completion date
Unknown
Last updated
2007-12-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Micturition Disorder

Brief summary

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

Detailed description

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.

Interventions

PROCEDUREClinical and functional examination (uroflowmetry, bladder scan and video-urodynamic examination)
BEHAVIORALAdaptation of the drinking scheme
BEHAVIORALMicturition clock

Sponsors

University Hospital, Ghent
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Known neurogenic bladder disorder

Design outcomes

Primary

MeasureTime frame
Prevalence of micturition disorders
Etiology of micturition disorders after 10 weeks observation
Influence of drinking scheme on bladder capacity and micturition continence after 10 weeks observation

Secondary

MeasureTime frame
Efficacy of the therapy after 3, 6, 9, 12 months

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026