Comparison of intravenous, local and oral Tranexamic Acid effect on reducing postoperative bleeding ?in coronary artery bypass graft surgery

Phase 3

Recruiting

• Conditions: Coronary artery bypass graft surgery.; Mechanical complication of coronary artery bypass graft and biological heart valve graft; T82.2

• Registration Number: IRCT20141209020258N166
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 96

Inclusion Criteria

All elective patients are candidates for coronary artery bypass graft surgery
Lack of sensitivity to Tranexamic Acid

Exclusion Criteria

Death of patients
Reluctance to participate in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Bleeding. Timepoint: Within 24 hours. Method of measurement: Observation.;Count of platelet received. Timepoint: Within 24 hours. Method of measurement: Count.;Number of fresh frozen plasma received. Timepoint: Within 24 hours. Method of measurement: Count.;Number of pack cell received. Timepoint: Within 24 hours. Method of measurement: Count.;Mortality. Timepoint: Within 72 hours. Method of measurement: Observation.