NCT03572309

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

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 28 (actual)
• Sponsor: Masaryk University · Academic / Other
• Sex: All
• Age: 18 Years – 80 Years
• Healthy volunteers: Not accepted

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.

Detailed description

The study will commence following the Approval by The Ethics Research Committee. All patients admitted to emergency department during the study will be enrolled after fulfilling the inclusion criteria and in the absence of any exclusion criteria. Informed consent will be requested. After admission to emergency department the blood samples will be taken and blood tests and viscoelastic tests will be performed. All data and results will be entered in the study form. Statistical analysis will be performed and incidence of trauma induced coagulopathy estimated. In addition, 28-day mortality and the incidence of thromboembolic complications will be monitored.

Conditions

• Trauma
• Hemorrhage
• Coagulopathy

Timeline

• Start date: 2018-06-19
• Primary completion: 2023-04-04
• Completion: 2023-05-01
• First posted: 2018-06-28
• Last updated: 2025-05-14

Locations

1 site across 1 country: Czechia