Effect van Mirabegron op de urethrale druk tijdens urodynamisch onderzoek
Recruiting
- Conditions
- urinary urgency, urinarinary incontinence, over active bladder symptoms
- Registration Number
- NL-OMON26653
- Lead Sponsor
- P. Groenendijk, Medisch Centrum Haaglanden, den haag
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 75
Inclusion Criteria
Female patients, above age of 18, mentally fit to consent and indication for treatment with Mirabegron. Bothersome OAB symptoms. Voiding diary volume urine less then 2200ml.
•Signed informed consent
Exclusion Criteria
• Contraindications for the use of Mirabegron (severely impaired kidney- or liver function)
•Sediment + or clinical signs of UTI at the start of the urodynamic investigation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effect of mirabegron on urethral pressure variations
- Secondary Outcome Measures
Name Time Method