Catheter management bij symptomatische urineretentie na de bevalling.
Recruiting
- Conditions
- urinary retentionpostpartum periodcatheterretentionurinarykraamtijdurine retentieniet kunnen plassencatheter
- Registration Number
- NL-OMON27775
- Lead Sponsor
- Academic Medical Center, Amsterdam
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 84
Inclusion Criteria
1. Women who deliver in the participating hospitals;
2. Vaginally and by caesarean section;
Exclusion Criteria
1. Age < 18 years;
2. Insufficient knowledge or understanding of the Dutch language;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bladder related quality of life three months after randomization for symptomatic PUR (UDI-6 questionnaire)
- Secondary Outcome Measures
Name Time Method 1. Development of a risk profile for overt postpartum urinary retention;<br /><br>2. Prevalence of overt postpartum urinary retention (bladderscan);<br /><br>3. The prevalence of clinical urinary tract infections due to different catheterization methods;<br /><br>4. Cost effectiveness analysis for different treatments of overt PUR;<br /><br>5. Patient preference for different methods of catheterization.