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Clinical Trial Summary

The purpose of this project is to determine if a change in patient reported pain, nausea and vomiting after total knee arthroplasty can be observed with the substitution of a post operative adductor canal block for a preoperative adductor canal block in the current established peri-operative pain protocol and if these changes lead to a decrease in opioid consumption (in morphine equivalents).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05974501
Study type Interventional
Source University of Miami
Contact
Status Completed
Phase Phase 4
Start date September 29, 2023
Completion date January 22, 2024

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