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Overactive Bladder (OAB) Drink Advice Study

Not Applicable
Withdrawn
Conditions
Overactive Bladder Syndrome
Interventions
Dietary Supplement: water
Registration Number
NCT00982241
Lead Sponsor
Radboud University Medical Center
Brief Summary

The researchers want to investigate how fluid intake influences the symptoms of OAB. The researchers will recruit 45 patients with OAB and randomize them (blind) in 3 groups (low/normal/high fluid intake). Patients will follow this drink pattern for 2-5 days, while filling in an standard micturation diary for 2 days. This micturation diary is coupled to: collection of multiple urine samples, urine pH measurements, and a Perception of Intensity of Urgency Scale (PPIUS) scoring table. All this is collected by the patients themselves. Urine samples will be analysed for osmolality by the clinical chemistry department.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • OAB patients
Exclusion Criteria
  • benign prostatic hyperplasia
  • neurogenic detrusor overactivity
  • urine tract infection
  • anticholinergics
  • intravesical botulin toxin
  • cardiac failure
  • renal insufficiency
  • sacral neurostimulation
  • percutaneous neurostimulation

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
high fluid intakewater2400 ml/day (+/- 300 ml )for 2,5 days
low fluid intakewaterfluid intake 900 ml/day (+/- 300ml) for 2,5 days
normal fluid intakewater1500 ml /day (+/- 300 ml) for 2,5 days
Primary Outcome Measures
NameTimeMethod
PPIUS urge-score2 days
urine osmolality2 days
Secondary Outcome Measures
NameTimeMethod
PPIUS urge score2 days
urine pH2 days

Trial Locations

Locations (1)

Dept. of Urology, Radboud University Nijmegen Medical Centre

🇳🇱

Nijmegen, Gelderland, Netherlands

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