Rate of Catheter Colonization and Risk of Bloodstream Infection During Use of Two Different Central Venous Catheters (CVC)
Primary Purpose
Bacteriaemia, Catheter Related Bloodstream Infection
Status
Completed
Phase
Phase 4
Locations
Czech Republic
Study Type
Interventional
Intervention
central venous catheter
central venous catheter
Sponsored by
About this trial
This is an interventional prevention trial for Bacteriaemia focused on measuring central venous catheter, cvc, coated catheter, bacteriaemia, bloodstream infection
Eligibility Criteria
Inclusion Criteria:
- Patients with probable ICU stay
- Patient's first or second catheter placement during actual hospital stay
- Anticipated indwelling central venous catheter period >= 3 days (jugular vein, subclavian vein)
- >= 18 years of age
- Written informed consent of patient or independent physician prior to the participation; in this case: written informed consent after recovery if possible
Exclusion Criteria:
- The catheter will not be placed in the femoral vein
- Inflammation of the skin at the site of puncture prior to puncture
- Known hypersensitivity to any of the components (i.e. polyhexanide or related substances such as chlorhexidine)
- Participation in another clinical trial
- Emergency insertion of catheter in the field
Sites / Locations
- Faculty Hospital Brno
- Faculty Hospital Charles University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
coated central venous catheter
standard central venous catheter
Outcomes
Primary Outcome Measures
Incidence of catheter colonization
Incidence of bloodstream infection
Secondary Outcome Measures
Safety of catheter: complications related to the catheter and adverse events in general, clinical therapy, TISS-Score, ICU stay, infection markers
Safety of catheter: central venous catheter variables, time of catheter insertion and removal, kind of colonization
Full Information
NCT ID
NCT00555282
First Posted
November 7, 2007
Last Updated
February 4, 2010
Sponsor
B. Braun Melsungen AG
1. Study Identification
Unique Protocol Identification Number
NCT00555282
Brief Title
Rate of Catheter Colonization and Risk of Bloodstream Infection During Use of Two Different Central Venous Catheters (CVC)
Official Title
Rate of Catheter Colonization and Risk of Bloodstream Infection During Use of a Standard Central Venous Catheter (CVC) in Comparison to a Coated CVC
Study Type
Interventional
2. Study Status
Record Verification Date
February 2010
Overall Recruitment Status
Completed
Study Start Date
November 2005 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
July 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
B. Braun Melsungen AG
4. Oversight
5. Study Description
Brief Summary
The use of these catheters is associated with infectious complications that are an important iatrogenic source of morbidity and mortality. Certofix® protect is a catheter with a surface modified in order to reduce colonization by bacteria. This clinical trial is performed to compare the safety and efficacy of the coated central venous catheter, Certofix® protect, with that of the non-coated standard catheter Certofix®.
Detailed Description
Central venous catheters are an essential part of patient management in the ICU (Intensive Care Unit). The use of these catheters is associated with infectious complications that are an important iatrogenic source of morbidity and mortality. Many catheters become colonized with bacteria but only a proportion of colonised catheters go on to cause bacteriemia and sepsis. It is currently impossible to prospectively identify which of the catheters will become colonized and lead to sepsis. Various types of antiseptic or antimicrobial vascular catheter coatings have been developed. Studies showed that the coated catheters were effective in limiting the catheter colonization rate and that they may decrease the risk of catheter-related bloodstream infections. The "Certofix protect" was developed by B.Braun to reduce the risk of catheter related infections. It is a catheter with a modified surface that consists of a high molecular weight polymer which is non-covalently linked to the polyurethane catheter material. This clinical trial is performed to compare the safety and efficacy of the coated central venous catheter, Certofix® protect, with that of the non-coated standard catheter Certofix®.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bacteriaemia, Catheter Related Bloodstream Infection
Keywords
central venous catheter, cvc, coated catheter, bacteriaemia, bloodstream infection
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
680 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
coated central venous catheter
Arm Title
2
Arm Type
Active Comparator
Arm Description
standard central venous catheter
Intervention Type
Device
Intervention Name(s)
central venous catheter
Other Intervention Name(s)
Certofix Protect
Intervention Description
coated central venous catheter
Intervention Type
Device
Intervention Name(s)
central venous catheter
Other Intervention Name(s)
Certofix Trio
Intervention Description
standard central venous catheter
Primary Outcome Measure Information:
Title
Incidence of catheter colonization
Time Frame
after catheter removal
Title
Incidence of bloodstream infection
Time Frame
during treatment
Secondary Outcome Measure Information:
Title
Safety of catheter: complications related to the catheter and adverse events in general, clinical therapy, TISS-Score, ICU stay, infection markers
Time Frame
until discharge from ICU
Title
Safety of catheter: central venous catheter variables, time of catheter insertion and removal, kind of colonization
Time Frame
catheter removal
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with probable ICU stay
Patient's first or second catheter placement during actual hospital stay
Anticipated indwelling central venous catheter period >= 3 days (jugular vein, subclavian vein)
>= 18 years of age
Written informed consent of patient or independent physician prior to the participation; in this case: written informed consent after recovery if possible
Exclusion Criteria:
The catheter will not be placed in the femoral vein
Inflammation of the skin at the site of puncture prior to puncture
Known hypersensitivity to any of the components (i.e. polyhexanide or related substances such as chlorhexidine)
Participation in another clinical trial
Emergency insertion of catheter in the field
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jan Pachl, Prof. Dr.
Organizational Affiliation
Faculty Hospital Charles University Prague
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pavel Sevcik, Prof. Dr.
Organizational Affiliation
Brno University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty Hospital Brno
City
Brno
ZIP/Postal Code
662 43
Country
Czech Republic
Facility Name
Faculty Hospital Charles University
City
Prague
ZIP/Postal Code
100 00
Country
Czech Republic
12. IPD Sharing Statement
Citations:
PubMed Identifier
31142873
Citation
Krikava I, Kolar M, Garajova B, Balik T, Sevcikova A, Roschke I, Sevcik P. The efficacy of a non-leaching antibacterial central venous catheter - a prospective, randomized, double-blind study. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020 Jun;164(2):154-160. doi: 10.5507/bp.2019.022. Epub 2019 May 28.
Results Reference
derived
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Rate of Catheter Colonization and Risk of Bloodstream Infection During Use of Two Different Central Venous Catheters (CVC)
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