Could a steroid injection after knee surgery cut opioid use?
NCT ID NCT07151417
First seen Jun 26, 2026 · Last updated Aug 20, 2026 · Updated 2 times
Summary
This study tests whether adding a steroid to the standard pain injection during total knee replacement improves pain control and reduces the need for opioid painkillers. 240 adults undergoing knee replacement will be randomly assigned to receive either the standard injection, one with a traditional steroid, or one with a newer extended-release steroid. Researchers will track pain, opioid use, knee movement, and recovery for up to a year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- methylprednisolone and triamcinolone acetonide extended-release (Zilretta)
- What this could lead to
- If successful, this could point to a better way to manage pain after knee replacement, reducing opioid use and improving recovery.
- What could go wrong
- This is an early-to-mid-stage trial with 240 participants, so results may not apply to everyone. Steroids can affect blood sugar, especially in people with diabetes.
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 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 240 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
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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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Patients within the MHS who are DEERS eligible undergoing primary TKA at Walter Reed National Military Medical Center (WRNMMC), Surgery Center of Chevy Chase or District Surgery Center * Age 18 or older * successful surgical intervention Exclusion Criteria: * Unicompartmental knee arthroplasty (UKA) * Revision total knee arthroplasty (rTKA) * Females who are pregnant or nursing * Allergic to ingredients in PAI or previous adverse reaction to steroids being used in this study * Diabetics will be excluded from Group 2 (standard PAI + methylprednisolone)
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Walter Reed National Military Medical Center
RECRUITINGBethesda, Maryland, 20889, United States
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