DRKS00024211
Recruiting
Not Applicable
Comparison of uncoated central venous catheters with and without transient coating as product protection with regard to biofilm formation - CutSep
Solvamed GmbH0 sites852 target enrollmentFebruary 18, 2021
ConditionsPrevention of cathetersepsis
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Prevention of cathetersepsis
- Sponsor
- Solvamed GmbH
- Enrollment
- 852
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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