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RECRUITING
NCT05097976
PHASE4

Medrol Dosepak for Outpatient Total Knee Arthroplasty

Sponsor: Rush University Medical Center

View on ClinicalTrials.gov

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.

Official title: An Oral Methylprednisolone Taper Within a Multimodal Analgesic Regimen After Total Knee Arthroplasty: a Double-Blind Randomized Placebo-Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

420

Start Date

2022-03-01

Completion Date

2026-12

Last Updated

2025-04-29

Healthy Volunteers

Yes

Interventions

DRUG

Methylprednisolone

21 x 4mg tablets beginning on POD 1

DRUG

Placebo

21 sugar tablets beginning on POD 1 with standard management

Locations (1)

Rush Oak Brook Outpatient Center

Oak Brook, Illinois, United States