Comparison of ROTEM® derived parameters from venous and intraosseous blood
Not Applicable
- Conditions
- healthy probandsT79.2Traumatic secondary and recurrent haemorrhage
- Registration Number
- DRKS00007902
- Lead Sponsor
- Medizinische Universität Wien
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 23
Inclusion Criteria
Adult, healthy volunteers (male and female) without any known coagulation disorder; written informed consent; patients with polytrauma
Exclusion Criteria
•Ingestion of substances* known to influence coagulation tests
•Pregnancy
•breast-feading women
•age < 18à and > 99à
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method comparability of ROTEM derived Parameters of intravenous and intraosseous blood
- Secondary Outcome Measures
Name Time Method