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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00207779
Other study ID # E02
Secondary ID
Status Completed
Phase Phase 3
First received September 13, 2005
Last updated September 19, 2007
Start date May 2005
Est. completion date August 2005

Study information

Verified date September 2007
Source Centre National de Greffe de Moelle Osseuse
Contact n/a
Is FDA regulated No
Health authority Tunisia: Ministère de la Santé Publique
Study type Interventional

Clinical Trial Summary

We, the researchers at Centre National de Greffe de Moelle Osseuse, have shown in a randomised study (in press), that a low dose of unfractionated heparin (100 IU/kg/daily) was safe and effective to prevent catheter-related bloodstream infection in patients with haemato-oncological disease.

The aim of this prospective randomised controlled trial is to compare the incidence of catheter-related bloodstream infection in 2 groups of patients with haemato-oncological disease:

- Group A: heparin impregnated catheters

- Group B: low-dose unfractionated heparin (100 IU/kg/daily)


Description:

Studies have shown that catheter-related infection may be due to fibrin deposition associated with catheters. Interventions designed to decrease fibrin deposition and thrombus formation have the potential to reduce catheter-related infections. Seven randomised studies have been performed to assess the safety and efficacy of heparin (either as an infusion or bonded to central venous catheter) on central venous catheter-related bloodstream infections. Although a meta-analysis of 4 studies looking at heparin either as an infusion or bonded to central venous catheter showed a strong trend for a reduction in catheter-related bloodstream infection with the use of heparin, these studies used variable definitions of catheter-related infections.

We have shown in a randomised study (in press), that low dose of unfractionated heparin (100 IU/kg/daily) was safe and effective to prevent catheter-related bloodstream infection in patients with haemato-oncological disease. The aim of this prospective randomised controlled trial is to compare the incidence of catheter-related bloodstream infection in 2 groups of patients with haemato-oncological disease:

- Group A: heparin impregnated catheters

- Group B: low-dose unfractionated heparin (100 IU/kg/daily)


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date August 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 4 Years to 60 Years
Eligibility Inclusion Criteria:

- Age between 4 and 60 years

- Short term non-tunneled percutaneous central venous catheter

Exclusion Criteria:

- Presence of a central venous catheter at admission

- Major blood coagulation disorders (platelet count < 50 x 10^9, disseminated intravascular coagulation)

- Absence of catheter-tip culture at the time of catheter removal

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Device:
heparin impregnated central venous catheters


Locations

Country Name City State
Tunisia Centre National de Greffe de Moelle Osseuse Tunis

Sponsors (1)

Lead Sponsor Collaborator
Centre National de Greffe de Moelle Osseuse

Country where clinical trial is conducted

Tunisia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of catheter-related bloodstream infection in 2 groups of patients with haemato-oncological disease
Primary Group A: heparin impregnated catheters
Primary Group B: continuous infusion of low dose unfractionated heparin (100IU/kg/d) through non-impregnated catheter.
Secondary Analysis of variables that may be significant for the development of catheter-related bloodstream infection (catheter-related thrombosis; age; underlying disease; side of venous puncture; duration of catheterization)
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