Could tylenol and ibuprofen replace steroids for sudden injuries?
NCT ID NCT07393503
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two short-term pain relief methods for acute musculoskeletal injuries: a steroid dose pack (methylprednisolone) versus a combination of acetaminophen (Tylenol) and ibuprofen (Motrin). Sixty adults with new injuries (less than 2 weeks old) will take one of the treatments for 6 days and report their pain and function. The goal is to see if the over-the-counter option works as well as the prescription steroid.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Methylprednisolone, Acetaminophen, Ibuprofen
- What this could lead to
- If this trial succeeds, it could show that a simple over-the-counter pain reliever combination works as well as prescription steroids for acute injuries.
- What could go wrong
- This is a small pilot study with only 60 participants, so results may not apply to everyone. The study is still enrolling and outcomes are based on self-reported pain, which can vary.
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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- 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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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: * Adults 18+ * Able to answer survey questions in English * MSK pain \> 3 on the VAS scale in any body part * Invited to participate by and enrolling clinician Exclusion Criteria: * \> 2 weeks from pain onset * Fractures * Active infections * Anaphylactic reaction to either medication (Oral Steroids, Ibuprofen, and/or Acetaminophen) * Currently taking anti-platelet agents (aspirin \</= 100/mg a day, clopidogrel, etc.) * Chronic Kidney Disease Stage 3 or worse * Uncontrolled diabetes (A1C above 9) * Currently taking oral anti-coagulants * History of bleeding ulcer * Cirrhosis * Taking daily prednisone * Chronic pain syndrome * Chronic pain medication (gabapentin, Lyrica, narcotics, etc.) * Pregnant Patients * Worker's Compensation Patients
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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UBMD Orthopaedics and Sports Medicine (716 Health)
Buffalo, New York, 14221, United States
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