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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00148005
Study type Interventional
Source University Hospital, Ghent
Contact
Status Completed
Phase N/A
Start date September 2004

See also
  Status Clinical Trial Phase
Completed NCT06260917 - The Effect of Urinating Through the Zipper or by Pulling Down the Trousers on Uroflowmetry Parameters in LUTS
Completed NCT05475093 - Impact Evaluation of Different Micturition Modes on Patients With Medullar Injury of Quality of Life and Their Occupations