Can a single steroid dose transform knee replacement recovery?
NCT ID NCT05018091
First seen Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time
Summary
This trial compares three doses of dexamethasone (4 mg, 8 mg, and 16 mg) given during total knee replacement surgery to see which one best reduces pain, opioid use, and nausea after the operation. Adults having a primary knee replacement and staying at least one night in the hospital are eligible. The study measures opioid consumption and pain scores over the first 48 hours, along with nausea and blood sugar levels, to find the safest and most effective dose.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Dexamethasone, a corticosteroid given intravenously during surgery
- What this could lead to
- If successful, this could identify the optimal dexamethasone dose to improve recovery after knee replacement, reducing pain and opioid use.
- What could go wrong
- The trial is testing different doses, and higher doses may increase risks like blood sugar spikes. Results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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438 people
The number who actually took part.
- Started
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Oct 2021
- Finished
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May 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age \> 18 years * Primary total knee arthroplasty * Patients staying at least one night in the hospital after surgery Exclusion Criteria: * Same day discharge Age \< 18 years Revision or partial total knee arthroplasty Corticosteroid use within 3 months prior to surgery Inflammatory arthritis Current systemic fungal infection Renal or liver failure Prior adverse reaction to corticosteroid Primary TKA requiring hardware removal
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Columbia University Irving Medical Center
New York, New York, 10032, United States
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Jefferson Philadelphia University and Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
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Mass General Brigham
Somerville, Massachusetts, 02145, United States
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Mayo Clinic Institutional Review
Rochester, Minnesota, 55902, United States
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NYU Langone Health
New York, New York, 10016, United States
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Rush University medical Center
Chicago, Illinois, 60612, United States
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Stanford University
Redwood City, California, 94063, United States
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University of California, San Francisco
San Francisco, California, 94158, United States
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University of Pennsylvania Perelman School of Medicine
Philadelphia, Pennsylvania, 19104, United States
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Washington University
St Louis, Missouri, 63110, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- What do knee replacement patients really need to know? a study asks them
- Prepping the knee before surgery: a new approach to better recovery
- Which nerve drug wins the battle against Post-Surgical knee pain?
- Can the right anesthesia get knee replacement patients moving faster?
- Can relaxation exercises boost recovery after knee replacement?
- Virtual reality may replace some sedatives during knee surgery