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Coagulation disorders in trauma patients

Coagulation disorders in trauma patients - ALARM-BLEEDING study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33294
Enrollment
120
Registered
2009-09-23
Start date
2009-11-25
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Traumatisch letsel accidental injury Traumatic injury

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Trauma patients treated by a trauma team that received medical care in the shock room Age > 18 years

Exclusion criteria

Exclusion criteria: Patients with haemostatic abnormalities or deficiencies

Design outcomes

Primary

MeasureTime frame
The incidence proportion of bleeding in trauma patients as reflected by blood transfusions and/or surgical- or radiological interventions to control bleeding.

Secondary

MeasureTime frame
* Level of comparison of INTEM clotting time and aPTT and FIBTEM and Clauss test for fibrinogen. * Age, gender, length, body weight, hematocrit, hemoglobin, leukocyte count, CRP, highest creatinine, ISS, predictive outcome scores * Temperature upon arrival at the emergency department and temperature dynamics over the first 24 hours post-trauma. * Level of fibrinolysis using ROTEM APTEM test * Tissue factor, thrombin, thrombin-antithrombin complexes (TAT), antithrombin III (AT III), D-dimers and protein C * Medicine use: use of drugs that influence coagulation * Administration of blood products and fluid, urine production

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)