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Clinical Trial Summary

To investigate the difference between an opiate sparing pain management protocol versus a standard opiate-based protocol following shoulder arthroplasty in the ninety day postoperative period regarding visual analog scores and oral morphine equivalents.


Clinical Trial Description

This is a single center, investigator initiated, prospective, randomized, controlled trial conducted among patients who have given voluntary consent to participate. Participation will last until the completion of the twelve weeks standard of care follow up visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04294680
Study type Interventional
Source Campbell Clinic
Contact
Status Completed
Phase N/A
Start date August 1, 2019
Completion date May 31, 2021

See also
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