Intraosseous Access During Pediatric Resuscitation

A Comparison of Four Intraosseous Access Devices With Standard Venous Catheterization During Child Cardiopulmonary Resuscitation Simulation: a Randomized Crossover Trial.

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02305511

Acronym

IOCPR

Enrollment

130

Registered

2014-12-02

Start date

2014-11-30

Completion date

2014-12-31

Last updated

2014-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest

Keywords

Catheterization, Peripheral

Brief summary

The purpose of this study was to compare the Jamshidi, the BIG, the Cook, the EZIO intraosseous devices to standard peripheral venous catheterization during pediatric resuscitation.

Interventions

DEVICEPeripheral venous catheterization

Cannulation using standard method

DEVICEJamshidi

intraosseous access using the Jamshidi device

DEVICEBIG

intraosseous access using the BIG device

DEVICECook

intraosseous access using the Cook device

DEVICEEZIO

intraosseous access using the EZIO device

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

Inclusion criteria

* give voluntary consent to participate in the study * minimum 1 year of work experience in emergency medicine * experienced emergency medical personnel - EMS-paramedics

Exclusion criteria

* not meet the above criteria * wrist or low back diseases

Design outcomes

Primary

Measure	Time frame
Success rate on first attempt	1 day

Secondary

Measure	Time frame	Description
Ease of use	1 day	Ease of use as reported by participants
Time to successfully perform	1 day	Time to successfully perform the intraosseous access

Countries

Poland

Contacts

Primary ContactAndrzej Kurowski

andrzejkurowski987@gmail.com+48500186225

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026