TXA in Revision Total Shoulder Arthroplasty
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- STATUS
- Recruiting
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- End date
- Nov 24, 2025
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- participants needed
- 82
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- sponsor
- NYU Langone Health
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.
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.
Details
| Condition | Arthropathy Shoulder |
|---|---|
| Treatment | Tranexamic Acid |
| Clinical Study Identifier | NCT04650698 |
| Sponsor | NYU Langone Health |
| Last Modified on | 7 October 2022 |
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