EZIO Compared to Central Venous Lines for Emergency Vascular Access

Not Applicable

Withdrawn

• Conditions: Catheters, Indwelling; Central Venous Line; Intraosseous Needle
• Interventions: Device: standard central line; Device: Powered Intraosseous device (EZIO)

• Registration Number: NCT00785252
• Lead Sponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2008-09
• Study First Submitted: 2008-11-03
• Study First Submitted QC: 2008-11-03
• Study First Posted: 2008-11-05
• Primary Completion: 2010-09
• Study Completion: 2010-09
• Status Verified: 2021-09
• Last Update Submitted: 2021-09-22
• Last Update Posted: 2021-09-28

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
2	standard central line	Central line
1	Powered Intraosseous device (EZIO)	EZIO

Primary Outcome Measures

Name	Time	Method
Time taken to place the device	ED visit

Secondary Outcome Measures

Name	Time	Method
Incidence of complications	ED visit
Costs for each of the two methods	Ed visit

Trial Locations

Locations (1)

Dept of Emergency Medicine, The George Washington University Medical Center; 🇺🇸 Washington, District of Columbia, United States