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NCT07895472
Opioid Reduction and Enhanced Recovery in Orthopaedic Surgery (OREOS)-Knee
Conditions: Knee Arthroplasty, Total, Partial Knee Arthroplasty, Chronic Pain, Postoperative, Osteoarthritis (OA) of the Knee
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 170
Sponsor: McMaster University
Summary
Knee replacements are the second most common surgery in Canada. Most patients recover very well but research consistently shows that 1 in 5 patients still have pain many months after surgery. Doctors often prescribe opioid medications for pain after surgery (e.g. Percocet, hydromorphone, codeine). These medications can be helpful for some people, but they can also be dangerous, particularly when used for a long time. Many patients don't like the way opioids make them feel and would prefer alternative pain management strategies. Some people become addicted to opioids, have a difficult time reducing the dose of opioids, or have lasting health problems after using them. People in this study will be randomized to either have usual care or a new pathway designed to improve pain control and decrease opioid use after knee replacements. This study will have an intervention coordinator who will assess patients before surgery and who will follow up with patients regularly after surgery to make sure their pain is controlled and to avoid long-term opioid use. This study will use education, physiotherapy, psychological therapy, ice/cold, and non-opioid pain medications. As pain medications may work differently in different patients, the coordinator will check on each patient to look for pain control and assist to reduce the amount of opioids used after surgery. This study will help people have safer and more effective pain management after surgery which may lead to better recovery, higher satisfaction, and a lower risk of being harmed by opioids after surgery.
Eligibility Criteria
Inclusion Criteria:
* Adult (18+)
* Undergoing elective knee arthroplasty (total or partial) for knee arthritis
* Provide informed consent to participate
Exclusion Criteria:
* Revision surgery
* Simultaneous bilateral arthroplasties
* Inflammatory arthritis (like rheumatoid arthritis)
* Unable to consent (e.g., cognitive disability or substantial language barrier without a support person)
Source: ClinicalTrials.gov (NCT07895472). StuddyBuddy aggregates publicly available trial information.