Comparison of uncoated central venous catheters with and without transient coating as product protection with regard to biofilm formatio
Recruiting
- Conditions
- Prevention of cathetersepsis
- Registration Number
- DRKS00024211
- Lead Sponsor
- Solvamed GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 852
Inclusion Criteria
All patients should be included in the study, which:
- be supplied with uncoated central venous catheters
- have at least a catheter time of 60 hours
- have been given their consent and have understood the consent form
- are over 18 years old
Exclusion Criteria
Patients will not be admitted to the clinical trial if any of the following criteria are available:
- Catheter lying time less than 60 hours
- in front of lying the catheter, there are already positive blood culture evidence on the side of the clinic
- The absence of a signed declaration of consent
- Pregnant or breastfeeding women
- Patients after catheter change
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction of the number of biofilm positive peaks by at least 25%
- Secondary Outcome Measures
Name Time Method Improvement of the infectious aspects of the patient and the granting of the safety of the product