Overview

Goal-directed vs Preemptive Tranexamic Acid Administration in Total Hip Arthroplasty

Status:
Not yet recruiting
Trial end date:
2024-12-31
Target enrollment:
0
Participant gender:
All
Summary
The present study is a multi-center randomized prospective placebo-controlled non-inferiority trial. The study's primary objective is to compare the amounts of postoperative bleeding using two different TXA administration strategies: empirical TXA administration vs. viscoelastic test-based Goal-directed vs Preemptive Tranexamic Acid Administration in total hip arthroplasty. The secondary objectives include comparing the incidents of hyper-fibrinolysis, thromboembolic complications, and postoperative seizures. Researchers assumed that goal-directed tranexamic acid (TXA) administration using viscoelastic field tests would not be inferior to the empirical TXA administration strategy in reducing postoperative bleeding and hyper-fibrinolysis. It also would be beneficial in lowering TXA-induced thromboembolic complications and seizures.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Konkuk University Medical Center
Treatments:
Tranexamic Acid
Criteria
Inclusion Criteria:

Inclusion Criteria patients undergoing following surgery

- total hip arthroplasty

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