drugset / Trial / NCT05097976

Medrol Dosepak for Outpatient Total Knee Arthroplasty

NCT05097976

Phase 4 Recruiting 420 enrolled Rush University Medical Center
RandomizedParallel-groupDouble-blindPrevention

Summary

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.

Timeline

Start
2022-03-01
Primary completion
2027-05-30
Completion
2027-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylprednisolone Other / unclassified 4 mg Oral

Indications

No indication recorded.