CompletedPhase 3ACTRN12620001059954

Efficacy of perioperative Tranexamic Acid in patients undergoing trochanteric hip fracture surgery: A Randomized Placebo Controlled Trial.


Sponsor

Dr.Faaiz Ali Shah

Enrollment

184 participants

Start Date

Jan 2, 2021

Study Type

Interventional

Conditions

Summary

The purpose of the study will be to determine the effect of a single bolus dose of tranexamic acid, given intravenously at the beginning of the operation, on blood loss and need for blood transfusions in hip fracture surgery. Patients of intertrochanteric fractures undergoing DHS surgery will be divided into Two groups A(tranexamic acid) and group B(Placebo) and will receive 1 g of intravenous TXA mixed in 100 cc of saline, and an equivalent volume bolus of saline respectively at the time of surgical incision. Blood loss will be estimated based on the hemoglobin drop by measuring hemoglobin on consecutive measures, preoperative in the morning before surgery, 6 hours postoperative , 24 hours postoperative.,48 hours and 72 hours. The primary outcome of the study will be the rate of blood transfusion from the time of surgery until discharge at 72 hours post operatively. The secondary study outcomes include ,re operation and frequency of adverse events at 6 months follow up (including transfusion reaction, myocardial infarction, symptomatic DVT, pulmonary embolus, reoperation, readmission, wound infection and death) Our hypothesis is that the administration of Tranexamic acid (TXA) will decrease blood loss in hip fracture patients and lower the rate of allogenic blood transfusion.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria4

  • Patients of either gender 18 years and above.
  • Trochanteric fracture types AO 31-A1, A2.
  • Received within one week after sustaining the fracture
  • American Society of Anesthesiologists (ASA) scores of I & II

Exclusion Criteria10

  • Pre operative hemoglobin <10gm/dl.
  • Allergy to tranexamic acid
  • Severe dysfunction of heart, lung, liver, kidney, or coagulation.
  • Provoked deep venous thrombosis or pulmonary embolism within 30 days or myocardial infarction, cerebrovascular accident, or stent placement within 6 months.
  • Anticoagulant therapy such as antiplatelet drugs or warfarin before surgery.
  • Multiple fractures
  • Pathological fractures
  • Open fractures
  • Periprosthetic fractures
  • Pregnancy

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

Brief Name:Tranexamic Acid(TXA) usage in hip fracture surgery 1 gram of intravenous Tranexamic acid(TXA) mixed in 100 cc of saline, bolused at the time of surgical incision in operation theatre to

Brief Name:Tranexamic Acid(TXA) usage in hip fracture surgery 1 gram of intravenous Tranexamic acid(TXA) mixed in 100 cc of saline, bolused at the time of surgical incision in operation theatre to patients with dynamic hip screw fixation for intertrochanteric fractures.It will be administered by anaesthesist.Those assigned to the placebo group will receive an equivalent volume bolus of saline at the time of surgical incision. Peri operatively the transfusion trigger will be hemoglobin concentration equal to 9 g dl-1 for all patients.When these triggers are met whole blood will be transfused. Only for patients at risk (acute coronary syndrome, severe left ventricular dysfunction, or chronic respiratory failure), if hypotension could not be corrected despite adequate volume replacement during surgery and in case of syncope, transient ischaemic attack, stroke, acute respiratory failure, or acute coronary syndrome after surgery the transfusion trigger will be hemoglobin concentration of 10 g dl-1.During surgery, blood losses will be replaced with Ringer's lactate in a 3:1 ratio, with 6% hydroxyethyl starch 130/0.4 (Voluven, Fresenius Kabi, Bad Homburg, Germany) in a 1:1 ratio, or both until haemoglobin concentration fell bellow the transfusion trigger point. Thereafter, patients will receive 1 unit of allogeneic packed red cell hourly at a time until haemoglobin concentration raised above the transfusion trigger. Postoperative fluid therapy will be standardized for the first 12 hours. Each patient received 15 ml kg-1 of rehydration fluid (Na 40 mmol l-1, K 20 mmol l-1, glucose 250 mmol l-1).


Locations(1)

KHYBER PAKHTUNKHWA, Pakistan

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12620001059954