Medrol Dosepak for Outpatient Total Knee Arthroplasty

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorRush University Medical Center

About this trial

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.

Eligibility criteria

Qualifiers

Any patient undergoing primary TKA with a diagnosis of osteoarthritis

Willingness to undergo randomization

Disqualifiers

Reported chronic corticosteroid or opiate use

Suspected or confirmed periprosthetic joint infection

Revision TKA

Primary diagnosis other than osteoarthritis, including avascular necrosis, fracture, or post-traumatic arthritis

Trial design

Treatments tested in this trial

  • Methylprednisolone
  • Placebo

Treatment groups

420 Participants
are divided into 2 treatment groups

Sponsors and collaborators