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Clinical Trials/DRKS00024211
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

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.

Registry
who.int
Start Date
February 18, 2021
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Solvamed GmbH

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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