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Clinical Trials/NL-OMON35512
NL-OMON35512
Recruiting
Not Applicable

The effect of position (sit/stand up vs supine position) on urge sensation in volunteers and in patients with overactive bladder syndrome - The effect of position (sit/stand up vs supine position) on urge sensation

Academisch Ziekenhuis Maastricht0 sites100 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
overactive bladder syndrome
Sponsor
Academisch Ziekenhuis Maastricht
Enrollment
100
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational non invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patient arm: patients older than 18 years with OAB diagnosed by their urologist using the criteria of more than 8 micturitions on three consecutive days of these three days they keep a micturation diary with a VAS score for urge sensation. Patients should have at least one episode of urge: sudden compelling desire to void which can not be postponed.
  • Volunteers arm: volunteers older than 18 years are considered eligible if they have no urologic history or urinary complaints.

Exclusion Criteria

  • Patient arm: congestive heart disease or history of heart failure; patients on anticholinergic medication that are not willing to stop this medication; presence of post void residual urine \> 100cc determined by ultrasound; presence of urinary tract infection, determined by urine sticks. Patients with urinary tract infection will be treated by antibiotics. After resolution of the infection, the patient can re\-enter the study if the urine is sterile at that moment.
  • Volunteer arm: urinary complaints or urologic history; congestive heart disease or history of hear failure; presence of postvoid residual urine \> 100cc determined by ultrasound; presence of urinary tract infection, determined by urine sticks. Volunteers that present with urinary tract infection will be definitively excluded from participation.

Outcomes

Primary Outcomes

Not specified

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