CBD oil may curb chronic pain after knee surgery
NCT ID NCT03825965
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
About 25% of people who have knee replacement surgery develop persistent pain that can last for months. This trial tests whether taking a CBD-dominant oil before and after surgery can reduce that risk. Researchers will randomly assign about 40 adults to receive either CBD oil or a placebo, and follow them for six months. The main goal is to see if a larger study is feasible, but they will also track pain levels and opioid use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CBD-dominant oil (cannabidiol with a small amount of THC)
- What this could lead to
- If this pilot succeeds, it could lead to a larger trial testing whether CBD oil can prevent long-term pain after knee replacement, offering an alternative to opioids.
- What could go wrong
- This is a small pilot focused on feasibility, not proof of pain relief. CBD may cause side effects like drowsiness or liver issues, and 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
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
39 people
The number who actually took part.
- Started
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May 2023
- Finished
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Feb 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 undergoing TKA aged 18 or older * Cognitive ability and English-language skills required to complete outcome measures * Provision of informed consent * Successful completion of the run-in period Exclusion Criteria: * Severe cardio-respiratory disease (For operationalizing: ASA 4/NYHA 4) * Substance use disorder based on DSM-V criteria * Allergy or intolerance to cannabis, cannabis derivatives, or other ingredients of the study drug * Patients who are pregnant, planning to be pregnant, or breastfeeding * Revision TKA * Bilateral TKA * Presenting for their pre-surgical consultation less than 4 weeks before surgery * Patients with a chronic pain condition affecting the knee (other than osteoarthritis) (e.g.: patients with knee pain due to fibromyalgia or chronic pain syndrome will be excluded) * Unwilling or unable to follow the study protocol
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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
-
St. Joseph's Healthcare Hamilton
Hamilton, Ontario, L8N 4A6, Canada
-
St. Michael's Hospital
Toronto, Ontario, M5B 1W8, Canada
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Other studies related to the condition(s) this trial covers.
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