Status:

COMPLETED

Noninferiority Oral Tranexamic Acid vs Intravenous Administration in Total Hip Arthroplasty

Lead Sponsor:

University of Liege

Conditions:

Hemorrhage Postoperative

Total Blood Loss

Eligibility:

All Genders

18-90 years

Phase:

PHASE4

Brief Summary

To find noninferiority relationship between oral and intravenous administration of tranexamic acid on peroperative and postoperative blood loss and serum concentration during primary total hip arthrop...

Detailed Description

Tranexamic acid is an anti-fibrinolytic drug, recommended in total hip arthroplasty to reduce peroperative and postoperative hemorrhagic complications. The original character of our study lies in the ...

Eligibility Criteria

Inclusion

  • \- ASA physical status 1, 2 and 3 scheduled for primary total hip arthroplasty

Exclusion

  • Renal failure with serum creatinine level higher than 1,40 mg/dL
  • Thromboembolic events in last 12 months before surgery
  • Pregnancy
  • Congenital or acquired coagulation diseases
  • History of gastric surgery that could lead to malabsorption
  • Diabetic gastro-paresis

Key Trial Info

Start Date :

January 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 14 2022

Estimated Enrollment :

230 Patients enrolled

Trial Details

Trial ID

NCT04691362

Start Date

January 1 2021

End Date

December 14 2022

Last Update

December 15 2022

Active Locations (1)

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CHU de Liège

Liège, Belgium, 4000