Medrol Dosepak for Outpatient Total Knee Arthroplasty

This study is looking at whether a medication called methylprednisolone (a steroid often used to reduce inflammation) can help people recover from total knee replacement surgery (total knee arthroplasty or TKA) more comfortably. Researchers want to see if taking methylprednisolone starting the day after surgery reduces pain, opioid use, and nausea, and improves how well you can move your knee compared to a placebo (a sugar pill). You might be able to join if you are at least 18 years old, are having your first total knee replacement for osteoarthritis, and haven't used certain medications long-term. The study aims to enroll 420 participants, but its current recruitment status is unclear.

Study design
This is an interventional study comparing methylprednisolone to a placebo in 420 planned participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Opioid consumption will be measured at one week postoperative. Pain and functional outcomes will be assessed at 3 and 6 weeks postoperatively.

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NCT05097976

Medrol Dosepak for Outpatient Total Knee Arthroplasty

Recruiting
PHASE4Ages 18+InterventionalPrevention
Rush University Medical Center
~420 participants
Updated 2026-07-09 on ClinicalTrials.gov
What's tested:MethylprednisolonePlacebo

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Opioid consumption at one-week postoperative
Measured over one week
Total Knee Arthroplasty
1 sites across 1 states
Illinois1
  • Craig Della Valle, MD · PRINCIPAL_INVESTIGATOR · Rush University Medical Center

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Eligibility criteria

Inclusion

Any patient undergoing primary TKA with a diagnosis of osteoarthritis
Willingness to undergo randomization

Exclusion

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
American Society of Anesthesiologists (ASA) score ≥ 4
Reported history of liver disease, renal disease, or diabetes mellitus
Current systemic fungal infection or other local infection
Immunocompromised or immunosuppressed
Current peptic ulcer disease
History of hypothyroidism, psychosis, heart failure, myasthenia gravis, ocular herpes simplex virus, or systemic sclerosis
Women with reported current pregnancy
Known hypersensitivity to methylprednisolone
Inability to take oral medications
Unable to provide consent
  • Opioid consumption at one-week postoperativeone week

    Relative difference in cumulative opioid consumption at Post-op day 7, measured in morphine equivalents.