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study of effect of local Tranexamic acid in reducing postoperative bleeding on ?coronary artery bypass graft ?

Phase 2
Recruiting
Conditions
Coronary bypass graft.
Atherosclerosis of coronary artery bypass graft(s), unspecified, with angina pectoris
I25.70
Registration Number
IRCT20141209020258N62
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
62
Inclusion Criteria

Patients with elective CABG referrals
ASA Class 2 and 3
Tranexamic acid insensitivity
Surgery performed by a surgeon
Duration of surgery 4 to 6 hours

Exclusion Criteria

Increase the duration of the operation for more than 6 hours
cardiomegaly and CHF
Going on a cardio-pulmonary pump for 2 times during operation
All patients who die during surgery
History of cardiac arrest and CPR before surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bleeding after surgery. Timepoint: after surgery. Method of measurement: score.;Mean number of PACs received during 24 hours after surgery. Timepoint: 24 hours after surgery. Method of measurement: count.;Mean number of unit platelets received within 24 hours after surgery. Timepoint: 24 hours after surgery. Method of measurement: count.;Mean of number of FFP units received within 24 hours of surgery. Timepoint: 24 hours after surgery. Method of measurement: count.;The average number of returns to the operating room to control bleeding within 24 hours of operation. Timepoint: 24 hours after surgery. Method of measurement: count.
Secondary Outcome Measures
NameTimeMethod
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