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Observation of Intraosseous Vascular Access in the Emergency Department

NCT01235078 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 105

Last updated 2025-12-15

No results posted yet for this study

Summary

The purpose of this study is to evaluate the use of powered intraosseous vascular access (EZ-IO by Vidacare) in the emergency department for patients requiring urgent vascular access. Data collected will be compared to historical data on central venous catheter use in the emergency department. The primary hypothesis is that powered intraosseous vascular access will decrease the amount of time needed to obtain vascular access.

Conditions

  • Patients Requiring Urgent Vascular Access

Interventions

DEVICE

EZ-IO

powered intraosseous vascular access system

Sponsors & Collaborators

  • Vidacare Corporation

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2011-07-31
Completion
2011-07-31

Countries

  • United States

Study Locations

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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 NCT01235078 on ClinicalTrials.gov