Novel Device for Rapid Fluid Administration

Device Related Sepsis Clinical Trial

Official title: Fluid Administration With LifeFlow vs Push/Pull

Status Completed

Clinical Trial Summary

The aim of the study is to determine if a new device is more effective in fluid administration than devices currently used when resuscitating pediatric patients in septic shock. This study will take place in a simulation lab setting and will not include the use of patients.

Clinical Trial Description

In this study, participants will be randomized to one of three devices in a Pediatric Intensive Care Unit simulation setting. Each participant will be provided the device, a 1L NS bag, tubing and a 22g IV. In each scenario, the objective will be to administer 3 20cc/kg boluses within a 15 minute period to the simulated patient. ;

Related Conditions & MeSH terms

• Device Related Sepsis

• NCT number: NCT03074682
• Study type: Interventional
• Source: Yale University
• Status: Completed
• Phase: N/A
• Start date: February 1, 2017
• Completion date: June 15, 2017