EZIO Compared to Central Venous Lines for Emergency Vascular Access

National Institutes of Health (NIH)

Status: Withdrawn

Conditions: Intraosseous Needle; Central Venous Line; Catheters, Indwelling

Treatments: Device: standard central line; Device: Powered Intraosseous device (EZIO)

Study type: Interventional

Funder types: Industry; NIH

Identifiers

NCT00785252

100731 (completed)

Details and patient eligibility

About

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.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

0 participants in 2 patient groups

1

Experimental group

Description:

EZIO

Treatment:

Device: Powered Intraosseous device (EZIO)

2

Experimental group

Description:

Central line

Treatment:

Device: standard central line