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Clinical Trials/NCT00785252
NCT00785252
Withdrawn
Not Applicable

Randomized Study of the EZIO Compared to Central Venous Lines Used for Emergency Vascular Access

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Catheters, Indwelling
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Locations
1
Primary Endpoint
Time taken to place the device
Status
Withdrawn
Last Updated
4 years ago

Overview

Brief Summary

Multicenter randomized study to compare powered intraosseous access to standard central line access for the administration of fluids and drugs for patients in the Emergency Dept.

Registry
clinicaltrials.gov
Start Date
September 2008
End Date
September 2010
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Over 18 years old Requires central access after peripheral access attempts have failed or are not otherwise feasible

Exclusion Criteria

  • Fracture in target bone Not able to sign informed consent Excessive tissue or absence of adequate anatomical landmarks Known or suspected coagulopathies Pregnancy Patients in custody Patients with suspected great vessel injury Not fluid in English

Outcomes

Primary Outcomes

Time taken to place the device

Time Frame: ED visit

Secondary Outcomes

  • Incidence of complications(ED visit)
  • Costs for each of the two methods(Ed visit)

Study Sites (1)

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