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Prehospital detection of hyperfibrinolysis in traumatized patients - a feasibility study

Prehospital detection of hyperfibrinolysis in traumatized patients - a feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021244
Enrollment
30
Registered
2020-04-02
Start date
2020-04-12
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

HYPERFIBRINOLYSIS POLYTRAUMA D65 T00-T07

Interventions

Group 1: ROTEM-analysis by a helicopter crew from traumatized patients prehospital and after arrival in hospital

Sponsors

Medizinische Hochschule Hannover Unfallchirurgie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Traumatized patients with subsequent transfer to the MHH by helicopter (Christoph 4)

Exclusion criteria

Exclusion criteria: Age <18 years; Pregnancy; Women during breastfeeding period

Design outcomes

Primary

MeasureTime frame
Detection of preclinical hyperfibrinolysis by means of rotational thrombo-stressometry (ROTEM), primarily via the LI30 (lysis index after 30 minutes) in comparison prehospital and after admission to hospital

Countries

Germany

Contacts

Public ContactChristian Macke

Medizinische Hochschule Hannover Unfallchirurgie

macke.christian@mh-hannover.de+4917615322533

Outcome results

None listed

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