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Efficacy of the fibrinogen and Fresh frozen plasma in patients with severe trauma

Phase 1
Conditions
Trauma.
Other early complications of trauma
Registration Number
IRCT2017051923559N13
Lead Sponsor
Vice chancellor for research, Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
40
Inclusion Criteria

Age over 18 years old; patients with multiple trauma; need for repeated transfusion; injury severity score 16 and above; satisfaction to participate in the study. Exclusion criteria: Unwillingness of the patient to continue cooperation in the plan; trauma limited to head; Penetrating trauma; injury severity score less than 16.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: 4 and 12 hours after the beginning of the intervention. Method of measurement: Manual blood pressure monitor.;Blood PH. Timepoint: 4 and 12 hours after the beginning of the intervention. Method of measurement: Lab.;Oxygenation index. Timepoint: 4 and 12 hours after the beginning of the intervention. Method of measurement: Lab.
Secondary Outcome Measures
NameTimeMethod
Types of brain and organ damage. Timepoint: At the beginning of the intervention. Method of measurement: Imaging through CT scan.;Level of consciousness. Timepoint: At the beginning of the intervention. Method of measurement: Using the Glasgow Coma Score.;Days requiring mechanical ventilation. Timepoint: During hospital admission. Method of measurement: Counting the days required for mechanical ventilation.;Number of blood units taken. Timepoint: During the days of admission. Method of measurement: Count of injected blood units.;Duration of hospitalization. Timepoint: Time of discharge. Method of measurement: Count the number of admitted days.;Patients death. Timepoint: End of intervention. Method of measurement: Clinical.
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