Trial Comparing Proximal Tibia and Proximal Humerus Infusion Rates Using the NIO Intraosseous Device (IOACS)

Medical University of Warsaw

Status: Completed

Conditions: Intraosseous Access; Resuscitation

Treatments: Device: NIO

Study type: Interventional

Funder types: Other

Identifiers

NCT02700867

02.006.1MR

Details and patient eligibility

About

The investigators sought to compare the intraosseous access success rates of the proximal tibia and the proximal humerus using new Intraosseous access device "NIO" in an adult cadaver model during simulated resuscitation.

Enrollment: 84 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• give voluntary consent to participate in the study
• paramedics
• without previous experience in intraosseous devices

Exclusion criteria

• not meet the above criteria

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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84 participants in 2 patient groups

Proximal tibia

Experimental group

Description:

Assumption of intraosseous access into the proximal tibia. Simulation of continous resuscitation was carried out using a system of chest compression LifeLine ARM.

Treatment:

Device: NIO

Proximal humerus

Experimental group

Description:

Assumption of intraosseous access into the proximal humerus. Simulation of continous resuscitation was carried out using a system of chest compression LifeLine ARM.

Treatment:

Device: NIO