Winclove CLEAR for recurrent urinary tract infections in wome
- Conditions
- (Recurrent) Urinary Tract Infections / (Recidiverende) UrineweginfectiesCystitis / CystitisQuality of Life / Levenskwaliteit 
- Registration Number
- NL-OMON25899
- Lead Sponsor
- This study is performed at the research facility of CR2O by Prof. Dr. Eric Claassen (Principal Investigator) and Drs. Joost Flach (Coordinating Investigator).
- Brief Summary
The results of this study showed a significant improvement on the UTI-QoL questionnaire in the CLEAR group compared with control. No publication is available yet.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
In order to be eligible for inclusion, a subject must meet all
of the following criteria:
Exclusion Criteria
A potential subject who meets any of the following criteria will be
excluded from participation in this study:
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. The differences in QoL between treatment arms according<br>to UTI-QoL-questionnaire data and SF-36 scores after the<br>intervention period.<br /><br>2. The difference in UTI incidence between treatment arms,<br>as measured by the mean number of patient-reported UTI<br>episodes during the intervention period.<br /><br>3. The difference in UTI symptom severity between<br>treatment arms, as measured by mean Symptom & Burden<br>questionnaire scores during the intervention period.
- Secondary Outcome Measures
Name Time Method