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Study identifier: NCT05097976 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Medrol Dosepak for Outpatient Total Knee Arthroplasty

Condition: Total Knee Arthroplasty  ·  Sponsor: Rush University Medical Center

PhasePhase 4
Planned participants420
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The purpose of this study is to evaluate the efficacy of an oral methylprednisolone taper on acute postoperative pain, function, opioid consumption, nausea, and complications following outpatient total knee arthroplasty (TKA). We hypothesize that administration of an oral methylprednisolone taper starting on postoperative day 1 (POD 1) following TKA will be associated with improved pain and decreased opioid use, nausea, and complications at POD1-7, as compared to similar patients who receive placebo. Additionally, those taking methylprednisolone will report decreased pain and greater objective functional outcomes at 3 and 6 weeks postoperatively as compared to controls.

This description comes directly from the study's public registry record.

Talk to the study team

Anne DeBenedetti  ·  3124322468  ·  anne.debenedetti@rushortho.com

Always discuss trial participation with your own doctor first.

Locations (1)

Rush Oak Brook Outpatient CenterOak Brook, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05097976