Taurolidine Lock Solution in the Prevention of Catheter Related Bacteremia

Sponsor
Aarhus University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00735813
Collaborator
Danish Child Cancer Foundation (Other), TauroPharm (Industry)
129
1
2
53
2.4

Study Details

Study Description

Brief Summary

Children with cancer need a long term tunnelled central venous catheter (TCVC) for the entire duration of their treatment. TCVCs are locked with heparin when not in use. The most frequent complications of long term TCVC are catheter related blood steam infections. Taurolock is a new lock that is claimed to prevent the formation of luminal biofilm in TCVCs and has been demonstrated to eradicate infected CVCs. In this study the investigators will compare TCVCs locked with heparin with TCVCs locked with Taurolock. Hypothesis: Taurolock will diminish the number of CRBSI in children with cancer compared with children with heparin lock of their CVC.

Condition or Disease Intervention/Treatment Phase
  • Device: Taurolock
  • Device: Heparin
Phase 3

Detailed Description

The most frequent complications of long term TCVC are catheter related blood steam infections(CRBSI)often caused by microorganisms located in the biofilm formed on the inner surface of the TCVC after a short time. CRBSI may be lifethreatening, will need long term intravenous broad spectrum antibiotic therapy possibly combined with intraluminal antibiotic lock therapy. In spite of this CRBSI may often lead to the premature removal of the TCVC.

Several methods to prevent the occurrence of intraluminal microbial colonization have been investigated with no single method standing out as the optimal one.

There is a need for a simple and safe method of reducing the occurrence of CRBSI in immunocompromised children receiving chemotherapy for malignant diseases. Various catheter lock solutions in stead of using heparin have been investigated in experimental models. Taurolidine is a chemically modified amino acid with broad spectrum antimicrobial activity in vitro. It is claimed to prevent the formation of luminal biofilm in TCVCs in a CVC model and it has been demonstrated to eradicate infected CVC in a three reports with a total of 18 patients.

In a 24 months study of routine use of Taurolidine 1,25%/Sodium-Citrate 4% (TaurolockTM) a reduction of gram-positive CVC associated infections was demonstrated. The findings were not statistically significant due to relatively few patients.

There is a need of a larger study with more patients receiving Taurolock for locking the TCVC between use in order to test for a significant reduction of the occurrence of CRBSI. Furthermore there is a need for an in vivo demonstration of the reduction of biofilm formation in TCVCs locked with taurolock compared with TCVCs locked with heparin.

Study Design

Study Type:
Interventional
Actual Enrollment :
129 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
A Randomised Study of Taurolock for the Locking of Tunneled Central Venous Catheters in Children With Malignant Diseases.
Study Start Date :
Apr 1, 2008
Actual Primary Completion Date :
Sep 1, 2012
Actual Study Completion Date :
Sep 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: A

Tunneled central venous catheters locked with Taurolock

Device: Taurolock
When not in use the childrens tunneled central venous catheters are locked with the liquid Taurolock instead of heparin.

Active Comparator: B

Tunneled central venous catheter locked with heparin

Device: Heparin
When not in use the childrens tunneled central venous catheters are locked with heparin

Outcome Measures

Primary Outcome Measures

  1. Number of catheter related blood stream infections(CRBSI)in the Taurolock group vs the heparin group. Number of CRBSI/1000 CVC days in the Taurolock group vs the heparin group. Number of CVCs removed in the Taurolock group vs the heparin group [November 2010]

Secondary Outcome Measures

  1. Biofilm formation in the CVCs treated with Taurolock compared with the biofilm formation in the CVCs treated with heparin [February 2010]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children aged 0-17 years with malignant disease requiring a tunneled central venous catheter.
Exclusion Criteria:
  • No written consent from child or parents

Contacts and Locations

Locations

Site City State Country Postal Code
1 Childrens Department of Oncology A4, Aarhus Universityhospital, Skejby Århus N Denmark 8200

Sponsors and Collaborators

  • Aarhus University Hospital
  • Danish Child Cancer Foundation
  • TauroPharm

Investigators

  • Study Director: Henrik Schrøder, MD, Dr.med., Aarhus Universityhospital, Skejby

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Mette Møller Handrup, MD, PhD, Aarhus University Hospital
ClinicalTrials.gov Identifier:
NCT00735813
Other Study ID Numbers:
  • 17344
First Posted:
Aug 15, 2008
Last Update Posted:
Sep 5, 2012
Last Verified:
Sep 1, 2012
Keywords provided by Mette Møller Handrup, MD, PhD, Aarhus University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 5, 2012