Comparison of ROTEM® derived parameters from venous and intraosseous blood

Comparison of ROTEM® derived parameters from venous and intraosseous blood - ROTEM® i.o.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00007902

Enrollment

161

Registered

2015-04-07

Start date

2015-07-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

healthy probands T79.2

Interventions

Group 1: Part1 of the study: analysis of ROTEM derived parameters from venous and intraosseus blood in healthy subjects Group 2: Part2 of the study: analysis of ROTEM derived parameters from venous a

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult, healthy volunteers (male and female) without any known coagulation disorder; written informed consent; patients with polytrauma

Exclusion criteria

Exclusion criteria: • Ingestion of substances* known to influence coagulation tests • Pregnancy • breast-feading women • age 99à

Design outcomes

Primary

Measure	Time frame
comparability of ROTEM derived Parameters of intravenous and intraosseous blood	—

Countries

Austria

Contacts

Public ContactMarion Wiegele

AKH Wien Abteilung für Anästhesie, Intensivmedizin und Schmerztherapie

marion.wiegele@meduniwien.ac.at+43-1-40400/68200

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026