A Randomized Crossover Cadaver Trial Comparing Proximal Tibia and Proximal Humerus Infusion Rates Using the NIO Intraosseous Device During Simulated Cardiopulmonary Resuscitation Performed by Paramedics

Medical University of Warsaw1 site in 1 country84 target enrollmentFebruary 2016

ConditionsIntraosseous Access Resuscitation

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Intraosseous Access
Sponsor: Medical University of Warsaw
Enrollment: 84
Locations: 1
Primary Endpoint: Success rate
Status: Completed
Last Updated: 10 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The investigators sought to compare the intraosseous access success rates of the proximal tibia and the proximal humerus using new Intraosseous access device "NIO" in an adult cadaver model during simulated resuscitation.

Registry

clinicaltrials.gov

Start Date

February 2016

End Date

March 2016

Last Updated

10 years ago

Study Type

Interventional

Study Design

Crossover

Sex

All

Investigators

Sponsor

Medical University of Warsaw

Responsible Party

Principal Investigator

Łukasz Szarpak

Principal Investigator

Medical University of Warsaw

Eligibility Criteria

Inclusion Criteria

•give voluntary consent to participate in the study
•paramedics
•without previous experience in intraosseous devices

Exclusion Criteria

•not meet the above criteria

Outcomes

Primary Outcomes

Success rate

Time Frame: 1 day

Success rate of IO cannulation was defined as successful administration of infusion solutions via the performed IO access. Failure was defined as extravasation or unsuccessful (first) effort of IO insertion.