Alternative IntraOsseous DevicesRandomised controlled trial comparing 3 intraosseous methods.
Completed
- Conditions
- severely injured patients
- Registration Number
- NL-OMON23528
- Lead Sponsor
- Medirisk
- Brief Summary
Hartholt KA, Van Lieshout EMM, Thies WC, Patka P, Schipper IB. Intraosseous devices: a randomized controlled trial comparing three intraosseous devices. Prehosp Emerg Care 2010;14(1)6-13.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
1. Patients in acute life threatening situations, requiring assistance of a mobile medical team;
2. Intravasculair medical or fluid resuscitation is necessary and intravasculair access cannot be obtained after two attempts.
Exclusion Criteria
1. Childeren under the age of 1 year;
2. Patients with suspected sternumanomaly (only FAST1).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary endpoint: aspiration of bone marrow upon succesfull placement of a bone needle.<br>Primary parameter is: time required for successful placement.
- Secondary Outcome Measures
Name Time Method Secundary endpoint: complications of the bone needle used.<br>Secundary parameters are: complications, success rates, user friendliness, pain encountered by the patient.