Can CBD prevent chronic pain after knee surgery?

Cannabidiol to reduce persistent post-surgical pain following total knee arthroplasty: protocol for a multi-centre, randomized, controlled pilot trial.

Pilot and feasibility studies • • Moderately Relevant
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AI Summary

This pilot trial is testing whether cannabidiol (CBD), a non-intoxicating compound from cannabis, could help reduce persistent post-surgical pain in patients undergoing knee replacement surgery. The study is significant because 1 in 4 knee replacement patients develop chronic pain even after successful surgery, and current treatments often rely on opioids with their associated risks. Researchers will recruit 40 patients across multiple centers and randomly assign them to receive either MPL-001 (an oral CBD-dominant formulation) or placebo alongside standard post-operative care for 6 months.

The trial is designed first as a feasibility study to determine if a larger, definitive trial is possible. Key benchmarks include successfully recruiting 40 patients within 6 months, achieving ≥75% treatment adherence, and maintaining <15% loss to follow-up. Beyond these feasibility metrics, researchers will measure how CBD affects post-surgical pain intensity, opioid consumption (a major health concern), sleep quality, physical function, and emotional well-being. The study represents an important exploration of CBD's analgesic and anti-inflammatory properties as a potential alternative or complement to traditional pain management strategies following major orthopedic surgery.

If the pilot trial meets its feasibility targets, the researchers plan to immediately transition their pilot participants into a larger definitive trial to establish whether CBD is truly effective for preventing persistent post-surgical pain. This approach could accelerate research and eventually provide surgeons and patients with new evidence-based options for managing one of the most frustrating complications of knee replacement—chronic pain that persists long after the surgery heals.

📄 Original Abstract

Total knee arthroplasty (TKA) is commonly performed to reduce pain and improve functional limitations associated with late-stage osteoarthritis. However, 1 in 4 patients experience persistent post-surgical pain (PPSP); a complaint that is associated with higher peri-operative pain. Cannabidiol (CBD) possesses analgesic and anti-inflammatory properties that may reduce the risk of persistent pain among TKA patients. We designed a pilot trial to assess the feasibility of a definitive trial comparing CBT to placebo for reducing PPSP in patients undergoing TKA. We propose a randomized, controlled, pilot trial in which 40 patients scheduled to undergo TKA will be randomized to receive MPL-001 (an oral CBD-dominant formulation) or placebo, in addition to standard care. The feasibility outcomes of this pilot trial are as follows: (1) our ability to recruit 40 patients in 6 months, (2) achieve ≥75% treatment adherence among patients, and (3) <15% loss to follow-up. Secondary outcomes are the effects of MPL-001 relative to placebo on PPSP, opioid use, peri-operative pain interference, physical and emotional function, return to functioning, sleep, and adverse events (AEs) up to 6 months post-surgery. The results of our pilot study will inform the feasibility of a definitive trial to establish the effectiveness of CBD to reduce PPSP after TKA. If no major changes to our protocol are required, we will treat this study as a vanguard trial and enroll our pilot patients into a definitive trial. We prospectively registered our trial on ClinicalTrials.gov (identifier: NCT03825965) before enrolling any patients.

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