Effect of prophylactic fibrinogen on the need for perioperative blood transfusion in traumatic patients undergoing abdominal surgery
Not Applicable
- Conditions
- Injury of intra-abdominal organs.Injury of intra-abdominal organs
- Registration Number
- IRCT2016050220795N3
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
All trauma patients. Exclusion criteria: Patients having received fibrinogen or cryoprecipitate before operation, Patients with hereditary or acquired coagulopathies and history of allergy to fibrinogen concentrate.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Transfusion requirements. Timepoint: Before and after surgery. Method of measurement: Hemoglobin levels.
- Secondary Outcome Measures
Name Time Method Fibrinogen plasma level. Timepoint: Before and after surgery. Method of measurement: fibrinogen plasma level.