NCT01676350

Intraosseous Access in the Emergency Department for Patients With Failed Attempts at Intravenous Access: A Randomized Trial Examining Resource Utilization and Patient Satisfaction

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 22 (actual)
• Sponsor: WellSpan Health · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

By doing this study, the investigators hope to learn whether patients with difficult to obtain IV access who are treated with IO access are more satisfied with their care and have better outcomes. The investigators are specifically studying the time difference between groups and the difference in the number of attempts required to obtain vascular access and begin to treat with fluids and medications. The study will also measure patient satisfaction and procedural pain, the frequency of central line placement, the length of stay in the hospital and emergency department, and adverse events to intravascular access to determine whether IO access can improve these measures. The investigators hypothesize that the use of a protocol utilizing an IO device for select patients with failed IV access will reduce the time requirements to obtain vascular access, reduce the number of attempts needed to obtain IV access, reduce the ED LOS, and have no negative impact on patient satisfaction compared to the current ED practices.

Conditions

• Difficult Peripheral IV Access

Interventions

Type	Name	Description
PROCEDURE	IO access using EZ-IO®	IO line placed using an FDA-approved device called an EZ-IO®.

Timeline

• Start date: 2014-08-01
• Primary completion: 2015-05-01
• Completion: 2015-06-01
• First posted: 2012-08-30
• Last updated: 2022-03-23
• Results posted: 2022-03-08

Locations

2 sites across 1 country: United States