Can a common Anti-Inflammatory replace opioids after ACL surgery?
NCT ID NCT06973785
First seen Jun 27, 2026 · Last updated Aug 25, 2026 · Updated 2 times
Summary
This study compares two pain medicines after ACL knee surgery: ketorolac (a non-steroidal anti-inflammatory) and oxycodone (a narcotic). Thirty patients will be randomly assigned to one of the two drugs and tracked for how many narcotic pills they need. The goal is to see if ketorolac can effectively control pain while reducing or eliminating the need for opioids.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ketorolac (Toradol)
- What this could lead to
- If it works, this could offer a non-narcotic pain control option after ACL surgery, reducing reliance on opioids.
- What could go wrong
- This is a small, early-phase trial with only 30 participants, so results may not apply broadly. Ketorolac may not control pain as well as narcotics for some 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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jul 2025
- Expected to finish
-
Jun 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
-
15 to 55 years
- Sex
-
Anyone
- Healthy volunteers
-
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: 1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for the duration of the study 3. Male or female, aged 15-55 years 4. Primary Autograft ACL surgery 5. Ability to take oral medication and willingness to patriciate in a virtual 1 week follow-up pill count visit Exclusion Criteria: 1\. Any extensor mechanism dislocation or disruption 2. Multi-ligament injury that requires repair 3. Treatment with another investigational drug or other intervention concurrently or previously that would interfere with postoperative pain control 4. Psychiatric illness that impedes evaluation of pain and/or narcotics use 5. History of Chronic Kidney Disease 6. History of inflammatory arthritis, diabetes, or autoimmune disease 7. History of GI bleed or documented GI ulcer (diagnosed by endoscopy) 8. Allograft or revision of ACLR 9. Contraindications to ketorolac or opioids \-
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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
-
Cleveland Clinic
Strongsville, Ohio, 44136, United States
-
Cleveland Clinic Coral Springs
Coral Springs, Florida, 33067, United States
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Cleveland clinic sports medicine
Garfield, Ohio, 44125, United States
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Other studies related to the condition(s) this trial covers.
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