Skip to main content
Clinical Trials/NCT01680666
NCT01680666
Completed
Not Applicable

A Prospective Randomized Trial of Ultrasound Versus Landmark Guided Central Venous Access in Children

Stanford University2 sites in 1 country150 target enrollmentMay 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Need for Central Venous Access
Sponsor
Stanford University
Enrollment
150
Locations
2
Primary Endpoint
Success of Central Venous Cannulation at First Attempt
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The investigators hypothesized that, in children undergoing venous cannulation for central line placement by pediatric surgeons, ultrasound-guided cannulation leads to an increase in successful venous cannulation at first attempt compared to landmark guided cannulation.

Registry
clinicaltrials.gov
Start Date
May 2009
End Date
December 2011
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Matias Bruzoni

Principle Investigator

Stanford University

Eligibility Criteria

Inclusion Criteria

  • All patients between the ages of 0 and 18 years undergoing tunneled central venous line placement under general anesthesia

Exclusion Criteria

  • Preoperative proof of non-patency of central veins
  • coagulopathy
  • access site surgeon

Outcomes

Primary Outcomes

Success of Central Venous Cannulation at First Attempt

Time Frame: Up to 410 seconds

The count (%) of patients with successful central venous cannulation at first attempt is reported.

Secondary Outcomes

  • Patients With Arterial Punctures(Up to 410 seconds)
  • Patients With Complications(Up to 410 seconds)
  • Success of Central Venous Cannulation Within First Three Attempts(Up to 410 seconds)
  • Time to Successful Cannulation(Up to 410 seconds)

Study Sites (2)

Loading locations...

Similar Trials