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Effect of tranexamic acid on blood loss after coronary artery bypass grafting in patients treated with clopidogrel

Phase 2
Conditions
Bleeding after CABG.
Haemorrhage and haematoma complicating a procedure, not elsewhere classified
Registration Number
IRCT201309125381N8
Lead Sponsor
Vice-chancellor of Research Babol University Of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

patients undergoing on-pump CABG who received clopidogrel with their last ingestion less than5 days preoperatively.
Exclusion criteria: previous cardiac surgery; hematocrit less than 33%; platelet count less than 100,000/mL; or allergy to tranexamic acid; renal failure(cr>2), hepatic failure; history of bleeding diasthesis; abnormal coagulation test; previous cardiac surgerry.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bleeding after CABG. Timepoint: 24 houres. Method of measurement: Measuring mediastinal drainage into the chest bottle.
Secondary Outcome Measures
NameTimeMethod
Blood and blood products transfusion after CABG. Timepoint: 24 hours. Method of measurement: Measuring units of blood and blood products tranfused during and after CABG.
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