Comparison Of Allogenic Blood Transfusion Versus Routine Blood Transfusio
Not Applicable
- Conditions
- Blood Transfusion.Blood Transfusion (without reported diagnosis)
- Registration Number
- IRCT201012045313N1
- Lead Sponsor
- Vice Chancellor For Research And Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
All patients with open femoral fracture who schedule for surgery, ASA less than 3, hemoglobin more than 11
Exclusion criteria were Cardiac disease, impaired renal function, baseline hemoglobin <11 g/dl, low concentrations of coagulation proteins, inadequate vascular access, and the absence of appropriate monitoring capability and refusal of participating in study
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method eed to blood transfusion. Timepoint: perioperative. Method of measurement: bloody gasses and suction blood.
- Secondary Outcome Measures
Name Time Method PT. Timepoint: before anesthesia. Method of measurement: laboratory tests.;PT. Timepoint: after anesthesia. Method of measurement: laboratory tests.;Hb. Timepoint: before anesthesia. Method of measurement: laboratory tests.;Hb. Timepoint: after anesthesia. Method of measurement: laboratory tests.;Platelet. Timepoint: before anesthesia. Method of measurement: laboratory tests.;Platelet. Timepoint: after anesthesia. Method of measurement: laboratory tests.