search
Back to results

Central Venous Catheter Replacement Strategies in Adult Patients With Major Burn Injury (CARB)

Primary Purpose

Catheter-related Bloodstream Infection, Complication of Catheter

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
central venous catheter replacement (Arrowgard Blue plus Quad-Lumen CVC )
Sponsored by
Hospital Universitario Getafe
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Catheter-related Bloodstream Infection focused on measuring burns, catheter related bacteremia,, infection, central venous catheter,, catheter-related bloodstream, adult critically ill patients

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults (> 18 years old) admitted in a Critical Care Burn Center with a total body surface area (TBSA) greater than 20% and/or smoke inhalation injury.

Exclusion Criteria:

  • Adults admitted in a Critical Care Burn Center with a Do-Not-Resuscitate (DNAR) order due to severity of injuries.

Sites / Locations

  • Critical Care and Burn Unit, Hospital Universitario de GetafeRecruiting
  • Hospital de Cruces
  • Complejo Hospitalario Universitario de A Coruna

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

scheduled wire-guided every six days

Scheduled replacement every six days

replacement guided by clinical criteria

Arm Description

scheduled wire-guided every six days and a replacement of the catheter in a different place after 12 days from randomization.

Scheduled replacement every six days in a different location

re change of catheter strategy guided by clinical suspicious of catheter-related bacteremia and replacement of the catheter in a different location.

Outcomes

Primary Outcome Measures

Accumulative Incidence rate of catheter-related bacteremia

Secondary Outcome Measures

Accumulative incidence rate of catheter colonization
From date of randomization until the date of first documented progression or date of adverse event (pneumothorax, hemothorax)or death from any cause, whichever came first, assessed up to 18 months.
Mechanical complications of catheter insertion
Neumothorax, hemothorax, arterial puncture,

Full Information

First Posted
May 13, 2012
Last Updated
August 28, 2012
Sponsor
Hospital Universitario Getafe
search

1. Study Identification

Unique Protocol Identification Number
NCT01603914
Brief Title
Central Venous Catheter Replacement Strategies in Adult Patients With Major Burn Injury
Acronym
CARB
Official Title
Comparison of Three Strategies for Changing of Central Venous Catheters in Patients With Serious Burns for the Prevention of Catheter-associated Bacteremia: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Unknown status
Study Start Date
May 2012 (undefined)
Primary Completion Date
June 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitario Getafe

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this project is to answer the following questions: To determine the incidence of catheter related bacteremia (CRB) with three strategies of central venous catheter exchange in critically ill adult patients with major burn and to determine the regimen that will minimize the risk of bacteremia. To determine the incidence rate of catheter colonization in adult patients with major burns. The scientific knowledge to be acquired through this project is of likely benefit to the care of critically ill patients with burns injury as follows: The intention is to improve the outcomes in critically ill patients by minimizing one of the most frequent causes of infection in the Burn Intensive Care Unit, those from central venous catheters. Decreasing infections will decrease morbidity, decrease length of stay, decrease costs, and decrease mortality.
Detailed Description
Aim: To determine the incidence of catheter-related bacteremia (CRB) with three primary schedules of central venous catheter exchange in adult critically ill patients with major burn injury. Hypothesis: A strategy of catheter exchange according with clinical criteria will result in no more CRB compared with a routine catheter changes without guidewire exchange strategy or frequent guidewire exchange or frequent new-site replacement. Background: The intravenous catheter-related bacteremia (ICRB) is a nosocomial infection affecting patients admitted to intensive care and that leads to increased morbidity. Accumulative incidence rates of ICRB are 5.5 infections per 1000 catheters-day. Several strategies have been proposed to decrease of the rate of ICRB in critically ill patients. However, there is not agreement to recommend a replacement pattern of central venous catheters in adult critically ill patients with major burns as a strategy for the reduction in intravenous catheter-associated bacteremia. Objectives. To compare three strategies of replacement from central venous catheters for the prevention of ICRB. Find out the risk of mechanical complications associated with each strategy of central venous catheter replacement. Method. Randomized, multicenter clinical trial, single blind to compare three strategies for intravenous catheter replacement in patients with major burns: a scheduled wire-guided strategy every six days: second, a scheduled strategy of replacement every six days in a different punction and third, a re-change strategy guided by clinical criteria for suspicion of catheter-associated infection. Primary outcome: catheter colonization rate and rate of intravenous catheter-associated bacteremia. Secondarily, we calculate the incidence rate of colonization of central venous catheter and finally we will analyze the associated complications. This project requires enough patients to show a difference between three intervention groups. A significant decrease in infection rate would be from the current 20 infections per 1000 catheter days to approximately 15 per 1000 catheter days. This would require a minimum of 1000 catheter days per group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Catheter-related Bloodstream Infection, Complication of Catheter
Keywords
burns, catheter related bacteremia,, infection, central venous catheter,, catheter-related bloodstream, adult critically ill patients

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
1120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
scheduled wire-guided every six days
Arm Type
Experimental
Arm Description
scheduled wire-guided every six days and a replacement of the catheter in a different place after 12 days from randomization.
Arm Title
Scheduled replacement every six days
Arm Type
Experimental
Arm Description
Scheduled replacement every six days in a different location
Arm Title
replacement guided by clinical criteria
Arm Type
Experimental
Arm Description
re change of catheter strategy guided by clinical suspicious of catheter-related bacteremia and replacement of the catheter in a different location.
Intervention Type
Device
Intervention Name(s)
central venous catheter replacement (Arrowgard Blue plus Quad-Lumen CVC )
Other Intervention Name(s)
Catheter Related Bacteremia in Burns, CARBB study
Intervention Description
Routine practices for the type of catheter of each participating Unit will be respected. Multilumen central venous catheter will be used (i.e Arrowgard Blue plus Quad-Lumen CVC set). Impregnated Catheter with antiseptics or with antibiotics will be allowed.The anatomical locations selected for the replacement of central venous catheter are: subclavian vein, internal jugular vein, femoral vein and the change will be addressed according to the randomization. The dressing and maintenance of the catheter will be guided according with the Guides of The Centers for Disease Control and Prevention (CDCs) and a check-in lists will be fill in for each catheter. A pre-defined stratified analysis will be performed according with: type of catheter, participating unit, and insertion site.
Primary Outcome Measure Information:
Title
Accumulative Incidence rate of catheter-related bacteremia
Time Frame
participants will be followed for the duration of Burn Center stay, an expected lenght of stay average of 6 weeks (that represents the mean length of stay average in our BUrn Center in 2011)
Secondary Outcome Measure Information:
Title
Accumulative incidence rate of catheter colonization
Description
From date of randomization until the date of first documented progression or date of adverse event (pneumothorax, hemothorax)or death from any cause, whichever came first, assessed up to 18 months.
Time Frame
participants will be followed for the duration of Burn Center stay, an expected lenght of stay average of 6 weeks (that represents the mean length of stay average in our BUrn Center in 2011)
Title
Mechanical complications of catheter insertion
Description
Neumothorax, hemothorax, arterial puncture,
Time Frame
during the procedure of central catheter insertion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults (> 18 years old) admitted in a Critical Care Burn Center with a total body surface area (TBSA) greater than 20% and/or smoke inhalation injury. Exclusion Criteria: Adults admitted in a Critical Care Burn Center with a Do-Not-Resuscitate (DNAR) order due to severity of injuries.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Oscar Penuelas, MD
Phone
0034-916834982
Email
openuelas@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Miguel A De la Cal, MD
Phone
0034-916834982
Email
mcal@ucigetafe.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oscar Penuelas, MD
Organizational Affiliation
Critical Care Department and Burn Center. Hospital Universitario de Getafe, Madrid, Spain
Official's Role
Principal Investigator
Facility Information:
Facility Name
Critical Care and Burn Unit, Hospital Universitario de Getafe
City
Getafe
State/Province
Madrid
ZIP/Postal Code
28905
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Oscar Penuelas, MD
Phone
0034-916834982
Email
openuelas@gmail.com
First Name & Middle Initial & Last Name & Degree
Miguel A De la Cal, MD
Phone
0034-916834982
Email
mcal@ucigetafe.com
First Name & Middle Initial & Last Name & Degree
Inmaculada Alia, MD
First Name & Middle Initial & Last Name & Degree
Karen Gomez Mediavilla, MD
First Name & Middle Initial & Last Name & Degree
Marcos Varela
Facility Name
Hospital de Cruces
City
Barakaldo
State/Province
Vizcaya
Country
Spain
Individual Site Status
Active, not recruiting
Facility Name
Complejo Hospitalario Universitario de A Coruna
City
A Coruna
Country
Spain
Individual Site Status
Active, not recruiting

12. IPD Sharing Statement

Citations:
PubMed Identifier
17351437
Citation
Silver GM, Klein MB, Herndon DN, Gamelli RL, Gibran NS, Altstein L, McDonald-Smith GP, Tompkins RG, Hunt JL; Inflammation and the Host Response to Trauma, Collaborative Research Program. Standard operating procedures for the clinical management of patients enrolled in a prospective study of Inflammation and the Host Response to Thermal Injury. J Burn Care Res. 2007 Mar-Apr;28(2):222-30. doi: 10.1097/BCR.0B013E318031AA44.
Results Reference
background
PubMed Identifier
17631903
Citation
O'Mara MS, Reed NL, Palmieri TL, Greenhalgh DG. Central venous catheter infections in burn patients with scheduled catheter exchange and replacement. J Surg Res. 2007 Oct;142(2):341-50. doi: 10.1016/j.jss.2007.03.063. Epub 2007 Jul 12.
Results Reference
result
PubMed Identifier
15060765
Citation
Brun-Buisson C, Doyon F, Sollet JP, Cochard JF, Cohen Y, Nitenberg G. Prevention of intravascular catheter-related infection with newer chlorhexidine-silver sulfadiazine-coated catheters: a randomized controlled trial. Intensive Care Med. 2004 May;30(5):837-43. doi: 10.1007/s00134-004-2221-9. Epub 2004 Apr 2.
Results Reference
result
Links:
URL
http://www.ameriburn.org/
Description
The American Burn Association is dedicated to improving the lives of everyone affected by burn injury through patient care, education, research and advocacy.

Learn more about this trial

Central Venous Catheter Replacement Strategies in Adult Patients With Major Burn Injury

We'll reach out to this number within 24 hrs