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NCT00136097 Clinical Trial

Study on the Infection Risk of Long Dwell Period Catheters in High Risk Intensive Care Unit (ICU) Patients

Burns Clinical Trial

Official title:
Study on the Infection Risk of Long Dwell Period Catheters in High Risk ICU Patients

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00136097
Other study ID # 2004/266
Secondary ID
Status Terminated
Phase N/A
First received August 25, 2005
Last updated December 19, 2007
Start date August 2005
Est. completion date June 2006

Study information
Verified date December 2007
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This is an evaluation of the use of silver impregnated catheters in burn patients to reduce catheter colonisation compared to the standard central venous catheter without antiseptic activity.

Recruitment information / eligibility
Status Terminated
Enrollment 142
Est. completion date June 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Burn patient

- Placement of a new trilumen central venous catheter

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Device:
• Placement of a silver impregnated central venous catheter

Locations
Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Degree of colonisation of the central venous catheter at the moment of removal
Secondary Incidence of a catheter related blood stream infection during the presence of the catheter
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Terminated NCT00824681 - Effect of Music Therapy on Families of Burn Patients Phase 1
Terminated NCT00634166 - Effects of Therapy With Sulfamylon® 5% Topical Solution Compared to a Historical Control Group Phase 4
Terminated NCT00464386 - Continuous Glucose Monitoring (POC) in the ICU N/A
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