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Clinical Trial Summary

This is a phase IV, randomized, single-blind, single-center study comparing calculated total blood loss, surgical drain output and hematoma formation in patients who receive 2 doses of Tranexamic Acid (TXA) versus control group undergoing revision total shoulder arthroplasty. Patients will be randomized to either receive 2 doses of IV TXA, first dose prior to surgical incision and second dose given 3 hours later or to the control group, where no TXA will be administered.


Clinical Trial Description

The objectives of the study are to compare the effectiveness of IV TXA on reducing calculated total blood loss, surgical drain output and hematoma formation in patients undergoing revision total shoulder arthroplasty. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04650698
Study type Interventional
Source NYU Langone Health
Contact
Status Terminated
Phase Phase 4
Start date January 7, 2021
Completion date March 12, 2023

See also
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