Clinical Trials Directory

Trials / Completed

CompletedNCT02318940

Femoral Central Venous Access Comparison of 2 Methods

Comparison of Effectiveness and Safety of Two Methods for Installing Femoral Central Venous Catheters in Pediatric Intensive Care Units : Anatomical Method vs Ultrasound in Real Time.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
99 (actual)
Sponsor
University of Chile · Academic / Other
Sex
All
Age
1 Week – 15 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effectiveness and safety of the installation of femoral central venous catheter (CVC) ultrasound-guided real-time 2D versus the landmark method

Detailed description

STUDY DESIGN Multicenter prospective randomized study in pediatric intensive care units of the Roberto del Rio's hospital and Exequiel González Cortés' hospital. Patients from entering the study between the months of January/2015 to December/2015, after signing informed by their parents or legal guardian consent, this will be implemented by the resident PATIENTS Previous studies report an average success rate of 50% on the first attempt in the anatomical method, both children and adults. Sample size is determined to improve on a 30% success rate using the ultrasound method. For a power of 80% in relation to success at the first attempt and with a confidence level of 95%, a total of 50 patients per branch is determined. Method of randomization Using computer program the patient leaving 50 patients in the group with the anatomical method, and 50 patients in the ultrasound method are randomized . OPERATOR Both installation landmark and ultrasound guidance will be performed by 3 or 4 team doctors resident in each center , who count on ≥ 3 years of experience in ICU and training in ultrasound-guided access . DEFINITIONS * Successful cannulation: is considered successful installation when the guide is installed without difficulty in femoral vein. * Cannulation the first try: is considered successful when installing the CVC is accomplished by first transcutaneous passage to the glass needle . * Attempt to cannulation: considered attempt the passage of the needle without removing or redirect moving forward. Each successive removal or redirection with a forward motion is considered more a try. * Arterial puncture: Arterial puncture aspiration involves pulsatile arterial blood . * Rescue: After the fifth attempt in the landmark method will change the method under ultrasound guidance and is considered not successful cannulation. Result of not having puncture site is changed. INSTALLATION METHOD * Anatomical : In supine with external rotation and abduction of the lower extremity is located by palpating the femoral artery in the femoral triangle and punctured medial to this towards the navel to have reflux of venous blood. * Guided by ultrasound: Ultrasound is performed to verify the presence and proper position of a target vessel before puncturing the skin followed by real-time ultrasound to guide the needle tip during the lancing process. OUTCOME It was considered as primary outcome main installation on the first try , and secondary outcome cannulation success, number of attempts and , as a complication of the procedure, arterial puncture. Rescue will be used after the 5th attempt in the anatomical method that will change the method under ultrasound guidance . Failure to gain access shall be considered as successful cannulation and change of puncture site STATISTICAL ANALYSIS For statistical analysis the Stata 12.0 software was used. Continuous variables were analyzed using descriptive analysis of normal distribution with means and standard deviations , and continuous variables were not normally distributed and qualitative medians and percentiles. For the primary outcome will be used to varying dicomtómic Chi square method

Conditions

Interventions

TypeNameDescription
DEVICEcentral venous catheterinstallation of Central venous catheter ultrasound guided
DEVICEcentral venous catheterinstallation of Central venous catheter landmark guided

Timeline

Start date
2014-12-01
Primary completion
2016-05-01
Completion
2016-05-01
First posted
2014-12-17
Last updated
2017-03-30
Results posted
2016-12-15

Locations

2 sites across 1 country: Chile

Source: ClinicalTrials.gov record NCT02318940. Inclusion in this directory is not an endorsement.