Title

Blood Loss After Early TXA in Hip Fractures.
The Effects of the Timing of Tranexamic Acid Administration on Blood Loss in Hip Fractures.
  • Phase

    Early Phase 1
  • Study Type

    Interventional
  • Status

    Recruiting
  • Study Participants

    120
Our present study aims to initiate TXA administration immediately upon diagnosis of hip fracture in the Emergency Department. This will be a single blind randomized controlled trial comparing early administration of TXA in the ED in addition to perioperative dosing versus the standard perioperative administration only. The study population will include patients who have sustained a femoral neck, intertrochanteric, or subtrochanteric femur fracture and are undergoing surgical internal fixation or arthroplasty. We will prospectively compare the need for blood transfusion, total and hidden blood loss, postoperative complications, length of stay and readmission within 30 days.
Consent will be obtained for study enrollment from the patient or legal decision maker. The patient will then be randomized and stratified based on the fracture type, fixation method anticipated, and presence of anticoagulation.

Treatment drug and saline placebo will be blinded from the patient. Treatment arm patients will receive a dose of 10 mg/kg of TXA IV as soon as possible in the ED. They will then receive repeat doses prior to skin incision and again after the end of surgery. Control group will receive a placebo dose of normal saline in the ED and then the standard 10 mg/kg TXA doses prior to surgery and again after the end of surgery. The perioperative doses will not be blinded.
Study Started
Jul 06
2020
Primary Completion
Jul 31
2023
Anticipated
Study Completion
Jul 31
2023
Anticipated
Last Update
Jul 19
2022

Drug Tranexamic acid

10 mg/kg IV TXA in the ED, repeat doses before skin incision and in PACU

  • Other names: Early TXA

Drug Normal Saline

100 mL 0.9% normal saline in the ED, 10 mg/kg IV TXA before skin incision and in PACU

  • Other names: Control Placebo

Early TXA Experimental

Experimental group will receive 10 mg/kg IV TXA while in the Emergency Department, and repeat preoperative and postoperative doses.

Control Other

Control group will receive 100 mL 0.9% normal saline in the Emergency Department, and 10 mg/kg IV TXA before skin incision and again in post anesthesia care unit.

Criteria

Inclusion Criteria:

Femoral neck, intertrochanteric, subtrochanteric femur fracture
Age >18
Undergoing surgical stabilization or arthroplasty by any method as determined by attending surgeon

Exclusion Criteria:

Age <18
Concomitant fracture
Preoperative anemia needing blood transfusion before surgery
Severe comorbidity (active cancer, severe pulmonary disease, ESRD)
Allergy for tranexamic acid
History of acute thromboembolic event (Deep Vein Thrombosis, Pulmonary Embolism, Stroke, TIA) in the previous 12 months
Myocardial infarction in the previous 12 months
Renal function impairment (creatinine clearance <30 mL/min), or kidney transplant
History of hypercoagulability (Factor V Leiden, Protein C/S deficiency)
No Results Posted