None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Inclusion Criteria (1) Age 19 years or older (2) Patients scheduled for non-cardiac surgery with high bleeding risk Spinal fusion surgery at level 2 or above Artificial joint replacement: hip, knee, etc. Prostatectomy Cystectomy Hepatectomy Non-cardiac surgery with high bleeding risk (3) Signed consent to participate in the study
Exclusion criteria
Exclusion criteria: 2) Exclusion Criteria 1) Pregnant women 2) Patients who refuse blood transfusion 3) Patients receiving thrombin 4) Patients with a history of thromboembolism and familial hypercoagulable disease within 90 days 5) Patients with a history of myocardial infarction or ischemic stroke within 90 days 6) Patients with hypersensitivity to TXA 7) Patients with a history of convulsions and epilepsy 8) Patients undergoing dialysis for end-stage renal failure 9) Other patients deemed unsuitable for the study by the investigators 10) Patients already assigned to a study arm who develop additional intraoperative bleeding and subsequent change in whether or not to receive TXA, rendering prior arm assignment meaningless
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - CRT MA (mm) | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative TEG 6 test value changes: CK r-time (min), CK a-angle (°), CRT MA (%), CRT LY30 (%), CFF MA (mm) Postoperative changes: hemoglobin, platelet, central laboratory coagulation tests (if available) | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center