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Clinical Trials/NCT03282292
NCT03282292
Withdrawn
Not Applicable

Central Venous Catheter Insertion Site and Catheter Colonization and Bloodstream Infection in Pediatric Cardiac Surgery

IRCCS Policlinico S. Donato1 site in 1 countrySeptember 12, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Central Line-associated Bloodstream Infection (CLABSI)
Sponsor
IRCCS Policlinico S. Donato
Locations
1
Primary Endpoint
CVC colonization
Status
Withdrawn
Last Updated
2 years ago

Overview

Brief Summary

Randomized controlled trial comparing femoral vs internal jugular insertion site of central venous catheters (CVC) in newborns and infants undergoing cardiac surgery. The experimental hypothesis is that the jugular insertion site is superior to the femoral in terms of catheter colonization.

Detailed Description

Background: in adult patients, the femoral site of insertion of CVC is notoriously at higher risk of colonization and central-line associated bloodstream infection (CLABSI) than other sites (jugular or subclavian). In pediatric patients, the femoral site is more commonly used than in adult patients, but there is no sound data on catheter colonization and CLABSI related to the insertion site. The experimental hypothesis of this randomized controlled trial (RCT) is that the jugular insertion site is less likely to induce catheter colonization and CLABSI than the femoral site. Methods: 160 patients under 1 year and scheduled for cardiac surgery will be included in this RCT; patients will be randomly allocated to the jugular (J Group) or Femoral (F Group). CVC insertion will be performed by one out of three selected expert operators. The primary endpoint is the catheter colonization based on identification of bacterial grow into the catheter at removal time; CLABSI and CRBSI rate based on the same bacterial identification into the catheter tip and in the blood culture performed in case of signs and symptoms of infection. Secondary endpoints are mechanical complications defined as arterial puncture immediately identified during procedure, hemothorax and pneumothorax; and procedural difficulty during insertion defined as number of attempts, no guidewire progress, duration of the procedure (time from the completion of the sterile precaution barriers and the catheter fixation.

Registry
clinicaltrials.gov
Start Date
September 12, 2017
End Date
October 12, 2019
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
IRCCS Policlinico S. Donato
Responsible Party
Principal Investigator
Principal Investigator

Marco Ranucci

Director Clinical Research

IRCCS Policlinico S. Donato

Eligibility Criteria

Inclusion Criteria

  • Planned cardiac surgery Age \<1 year Eligibility for both insertion sites (jugular and femoral) for CVC Availability of at least one out of the three chosen expert operators

Exclusion Criteria

  • Emergency surgery Known vascular anatomic anomalies Previous cardiac surgery in the last 6 months No expert operator availability Intensive Care unit before surgery Central venous catheter inside at the time of randomization
  • Withdraw criteria (only for the first endpoint):
  • Impossibility to placement catheter in the selected site.

Outcomes

Primary Outcomes

CVC colonization

Time Frame: 14 days

CVC positive culture after removal

CRBSI

Time Frame: 14 days

Positive CVC culture and blood stream infection for the same organism

CLABSI

Time Frame: More than 48 hours

A laboratory-confirmed bloodstream infection where central line was in place for more than 48h.

Secondary Outcomes

  • Procedural difficulty(1 hour)
  • Mechanical complications(1 day)

Study Sites (1)

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