Observation of Intraosseous Vascular Access in the Emergency Department

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

105 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-04-30

Study Completion Date

2011-07-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Patients Requiring Urgent Vascular Access

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Intraosseous vascular access

subjects with urgent vascular access needs in whom intraosseous vascular access has been attempted and/or established.

EZ-IO

Intervention Type DEVICE

powered intraosseous vascular access system

Interventions

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EZ-IO

powered intraosseous vascular access system

Intervention Type DEVICE

Other Intervention Names

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EZ-IO by Vidacare, Powered intraosseous vascular access

Eligibility Criteria

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Inclusion Criteria

* Patients requiring vascular access who would otherwise receive a central venous catheter due to lack of other options.

Exclusion Criteria

* Fracture in target bone, or significant trauma to the site
* Excessive tissue and/or absence of adequate anatomical landmarks in target bone
* Infection in target area
* IO insertion in past 24 hours, prosthetic limb or joint or other significant orthopedic procedure in target bone

Eligible Sex

ALL

Accepts Healthy Volunteers

No