Common painkiller ibuprofen put to the test after joint surgery
NCT ID NCT05575700
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether taking ibuprofen for eight days after hip or knee replacement surgery is safe. Over 2,900 adults were randomly given either ibuprofen or a placebo. Researchers tracked serious problems like heart attack, stroke, blood clots, kidney failure, and bleeding for 90 days after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ibuprofen
- What this could lead to
- If ibuprofen is found safe, it could confirm a common painkiller as a standard option after joint replacement surgery.
- What could go wrong
- This is a completed Phase 4 trial, but results are not yet published. Ibuprofen can still cause stomach ulcers, kidney problems, or bleeding in some people.
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 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
2,904 people
The number who actually took part.
- Started
-
Apr 2023
- Finished
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Aug 2025
- Lead sponsor
-
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
-
18 years and older
- 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: * Patients scheduled for elective primary hip and knee arthroplasty. * Age ≥ 18 years. * Planned postoperative treatment with NSAID. * Negative pregnancy test for women in the fertile age. * Informed consent. Exclusion Criteria: * Unable to understand or speak Danish. * Allergy to or contraindications against ibuprofen.
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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
-
Aalborg University Hospital
Farsø, 9640, Denmark
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Bispebjerg Hospital
Copenhagen NV, 2400, Denmark
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Gentofte Hospital
Hellerup, 2900, Denmark
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Nordsjællands Hospital Hillerød
Hillerød, 3400, Denmark
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Næstved Hospital
Næstved, 4700, Denmark
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Odense University Hospital
Odense, 3900, Denmark
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Private Hospital Gildhøj
Brøndby, 2605, Denmark
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Silkeborg Regional Hospital
Silkeborg, 8600, Denmark
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Svendborg Hospital
Svendborg, 5700, Denmark
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Vejle Sygehus
Vejle, 7100, Denmark
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Zealand University Hospital
Køge, 4600, Denmark
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