Trials / Completed
CompletedNCT01235078
Observation of Intraosseous Vascular Access in the Emergency Department
An Observational Study of Intraosseous Vascular Access Compared to Central Venous Catheters in the Emergency Department
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 105 (actual)
- Sponsor
- Vidacare Corporation · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | EZ-IO | powered intraosseous vascular access system |
Timeline
- Start date
- 2010-04-01
- Primary completion
- 2011-07-01
- Completion
- 2011-07-01
- First posted
- 2010-11-05
- Last updated
- 2025-12-15
Locations
6 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01235078. Inclusion in this directory is not an endorsement.