Incidence of Trauma Induced Coagulopathy in Patients With Prehospital Administration of Fibrinogen

NCT03572309 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 28

Last updated 2025-05-14

No results posted yet for this study

Summary

The purpose of the study is to find out the incidence of trauma induced coagulopathy in patients with severe trauma who received fibrinogen prior admission to emergency department during prehospital care.

Conditions

Sponsors & Collaborators

  • Brno University Hospital

    collaborator OTHER
  • Masaryk University

    lead OTHER

Principal Investigators

  • Roman Gal, MD, PhD · Masaryk University

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-06-19
Primary Completion
2023-04-04
Completion
2023-05-01

Countries

  • Czechia

Study Locations

More Related Trials

Entities

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 NCT03572309 on ClinicalTrials.gov