MedTrace Logo

Intraosseous Access

NCT02275520 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 137

Last updated 2015-05-13

No results posted yet for this study

Summary

The investigators will compare the success rates and time to successful IO access during simulated adult resuscitation.

Conditions

  • Intraosseus Access
  • Manikin
  • Resuscitation

Interventions

DEVICE

NIO Adult device

IO access-1

DEVICE

Bone Iniection Gun

IO access-2

DEVICE

EZ-IO

IO access-3

DEVICE

Jamshidi Intraosseous Needle

IO access-4

DEVICE

Cook Intraosseous Needle

IO access-5

Sponsors & Collaborators

  • International Institute of Rescue Research and Education

    lead OTHER

Principal Investigators

  • Lukasz Szarpak · National Institute of Cardiology, Warsaw, Poland

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2015-04-30
Completion
2015-05-31

Countries

  • Poland

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02275520 on ClinicalTrials.gov