Implementation of an Empiric Transfusion Bundle for Out of Hospital Patients With Haemorrhagic Shock

NCT06891131 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2025-12-17

No results posted yet for this study

Summary

The investigators will evaluate the implementation of a treatment bundle (Fibrinogen, Plasma and Tranexamic Acid)

Conditions

  • Haemorrhagic Shock
  • Trauma Coagulopathy

Sponsors & Collaborators

  • Medical University of Graz

    lead OTHER

Principal Investigators

  • Gabriel Honnef, MD, PhD · Medical University of Graz, Department of Anaesthesiology

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-01
Primary Completion
2027-04-01
Completion
2027-06-01

Countries

  • Austria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06891131 on ClinicalTrials.gov