A randomized clinical trial of urinary incontinence in older women: cost-effectiveness of protocolized assesment and evidence-based treatment.

niversity Medical Center Groningen (UMCG)0 sites246 target enrollmentTBD

Conditionsrinary incontinence (NLD: incontinentie voor urine).

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: rinary incontinence (NLD: incontinentie voor urine).
Sponsor: niversity Medical Center Groningen (UMCG)
Enrollment: 246
Status: Recruiting
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

2 years ago

Study Type

Interventional

Investigators

Sponsor

niversity Medical Center Groningen (UMCG)

Eligibility Criteria

Inclusion Criteria

•The source population consists of women aged 55 or older who are registered in the practices of 26 general practitiones in the northern part of The Netherlands. Patients are eligible for the study if the have symptoms of involuntary loss of urine, if they are able to fill in a questionnaire in Dutch and if they have given informed consent.

Exclusion Criteria

•Patient will be excluded if they have urinary tract infections or overflow incontinence, are suffering from malignancies, are currently treated for urogynaecological conditions, have an indwelling catheter or are severely demented or in a poor physical condition.

Outcomes

Primary Outcomes

Not specified

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