Goal-directed vs. Empirical Tranexamic Acid Administrationin Cardiovascular Surgery
Heart Diseases, Vascular Diseases, Transfusion Related Complication
About this trial
This is an interventional diagnostic trial for Heart Diseases
Eligibility Criteria
Inclusion Criteria: patients who will undergo elective cardiovascular surgery employing cardiopulmonary bypass patients who provide written informed consent Exclusion Criteria: pregnancy refusal of allogenic blood transfusion taking thrombin history of thromboembolic and familial hypercoagulability disease recent history of myocardial infarction or ischemic cerebral infarction (within 90 days) hypersensitive to TXA histroy of convulsion or epilepsy taking hemodialysis history of Heparin-induced thrombocytopenia
Sites / Locations
- Asan Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Active Comparator
Experimental
Experimental
Empirical 1: TXA and Placebo administration
Empirical 2: TXA administration
Goal-directed 1: Placebo administration
Goal-directed 2: TXA and Placebo administration
Tranexamic acid administration, regardless of the result of rotational thromboelastometry. Placebo administration, at LI60 < 85 % or A10< 40 mm in EXTEM of rotational thromboelastometry
Tranexamic acid administration, regardless of the result of rotational thromboelastometry. Placebo discard, at LI60 ≥ 85% or A10 ≥ 40 mm in EXTEM of rotational thromboelastometry
Placebo administration, regardless of the result of rotational thromboelastometry. Tranexamic acid administration at LI60 < 85 % or A10 < 40 mm in EXTEM of rotational thromboelastometry
Placebo administration, regardless of the result of rotational thromboelastometry. Tranexamic acid discard at LI60 ≥ 85% or A10 ≥ 40 mm in EXTEM of rotational thromboelastometry