Actively Recruiting

Phase 4
Age: 60Years +
All Genders
NCT03063892

Effect of Tranexamic Acid (TXA) on Reduction of Postoperative Blood Transfusion

Led by Gregory M Georgiadis MD · Updated on 2025-08-07

200

Participants Needed

1

Research Sites

469 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Tranexamic Acid (TXA) is an antifibrolytic medication used in total hip and knee arthroplasty to reduce the need for intraoperative and postoperative blood transfusions. Limited research is available on its use in hip fracture patients. We hypothesize that the use of TXA preoperatively, perioperatively, and postoperatively will decrease blood loss and need for blood transfusion postoperatively.

CONDITIONS

Official Title

Effect of Tranexamic Acid (TXA) on Reduction of Postoperative Blood Transfusion

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Over the age of 60 years
  • Hip fracture requiring surgical intervention
  • Signs consent and agrees to participate
Not Eligible

You will not qualify if you...

  • Under the age of 60
  • Does not sign consent or refuses participation
  • Known hypersensitivity to tranexamic acid
  • Multiple acute fractures
  • Creatinine clearance <30
  • History of seizures
  • Active hormone therapy
  • History of coagulation abnormality
  • History of deep vein thrombosis (DVT) or pulmonary embolism (PE) within the last year or history or recurrent DVT/PE
  • Myocardial infarction (MI) and/or stents within the past year
  • History of intracranial hemorrhage
  • Acquired defective color vision
  • Patients admitted directly to nursing units or surgery without stay in the Emergency Center
  • Patients who sustain fracture while hospitalized at ProMedica Toledo Hospital

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

ProMedica Toledo Hospital

Toledo, Ohio, United States, 43606

Actively Recruiting

Loading map...

Research Team

K

Kristin Gardner, MSN, RN

CONTACT

M

Michelle Barhite, RPh

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here