drugset / Trial / NCT04488367

Blood Loss After Early TXA in Hip Fractures.

NCT04488367

Phase 0 Unknown 120 enrolled Community Memorial Health System
RandomizedParallel-groupSingle-blindTreatment

Summary

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.

Timeline

Start
2020-07-06
Primary completion
2023-07
Completion
2023-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tranexamic Acid Small molecule 10 mg/kg Intravenous

Indications