Clinical Trials Directory

Trials / Unknown

UnknownNCT04855877

Oral Administration of Tranexamic Acid in Anterior Cruciate Ligament Surgery Reduce Postoperative Haemarthrosis

Does Oral Administration of Tranexamic Acid in Anterior Cruciate Ligament Arthroscopic Surgery Reduce Postoperative Haemarthrosis and Improve Functional Prognosis?

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
104 (estimated)
Sponsor
University of Liege · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

To find superiority relationship between oral and intravenous administration of tranexamic acid on peroperative and postoperative blood loss, haemarthrosis prevalence and improvement functional prognosis in anterior cruciate ligament arthroscopy.

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 serum dosage of tranexamic acid, allowing to correlate the primary objective (blood loss) with this one. The investigators will focus on the reduction of the risks associated with the administration of intravenous medicines, the economic aspect and the ease of use.

Conditions

Interventions

TypeNameDescription
DRUGOral tabletOral administration of 2 grammes tranexamic acid 2 hours before skin incision and 2 grammes oral tranexamic acid 4 hours after first administration
DRUGPlaceboOral administration of lactose tablet (placebo)

Timeline

Start date
2021-07-06
Primary completion
2023-06-01
Completion
2023-07-01
First posted
2021-04-22
Last updated
2021-07-28

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT04855877. Inclusion in this directory is not an endorsement.