Pain, Joint, Pain, Postoperative, Total Knee Arthroplasty
Conditions
Brief summary
Total knee arthroplasty (TKA) is one the most common surgical treatments performed for end stage degenerative arthritis of the knee. More than 700,000 procedures are currently performed yearly in the United States. This procedure usually results in moderate-to-severe pain in the immediate post-operative period. Optimal pain control may allow early mobilization, accelerate rehabilitation, improve patient satisfaction, decrease length-of-stay, and optimize functional outcomes. The challenge, however, is to manage pain with alternative methods, reducing the role of opiate medications, which are highly addictive with myriad side effects. In this prospective randomized double-blinded controlled study, the investigators aim to evaluate the benefits of an over-the-counter (OTC) transdermal CBD preparation in patients undergoing primary total knee arthroplasty as a novel adjunct to the standard multi-modal analgesic regimen, to reduce postoperative pain and reduce the need for opiates after total knee arthroplasty.
Interventions
DRUGCBD
CBD oil Roll-On Stick
DRUGMineral Oil
Mineral Oil- Roll on Stick
DRUGPlacebo
Roll- On stick with no CBD and no Mineral Oil
Sponsors
Rothman Institute Orthopaedics
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
1. Patients who have general anesthesia 2. Patients who have documented allergic reactions to ropivacaine in the local infiltration agents 3. Patients who have a contra-indication to the use of non-steroidal anti-inflammatory medications or are using therapeutic anticoagulation precluding them from using non-steroidal anti-inflammatory medications 4. Patients unable to complete a 100-ft walk baseline 5. Patients undergoing total knee arthroplasty as a conversion procedure following previous surgery 6. Patients undergoing TKA for posttraumatic arthritis 7. Patients undergoing TKA for steroid-induced or spontaneous avascular necrosis 8. Workers compensation patients 9. Patients refusing or not candidates for peripheral nerve blocks 10. Patients undergoing unicompartmental knee arthroplasty 11. Patients undergoing patellofemoral arthroplasty 12. Patients undergoing bilateral simultaneous or sequential primary total knee arthroplasty within the same hospital stay 13. Patients who have previously reported allergy to tetrahydrocannabinol or other cannabinoid compounds or develop allergic reactions to the formulation following use 14. Patients who are pregnant or choosing to be pregnant during the 6-week study period or are breast feeding during the study period 15. Patients who are on chronic narcotics pre-operatively 16. Patients who have end-stage cirrhosis, end-stage renal failures, or psychiatric conditions preventing adequate assessment of study outcome metrics 17. Patients with adequate cognitive function to participate and complete questionnaires for the study. 18. Patients unable or unwilling to follow-up and complete questionnaires for the study 19. Patients with active cancer and undergoing treatment precluding the assessment of outcome metrics 20. Patients with a history or diagnosis of chronic pain syndrome or Complex regional pain syndrome (CRPS) 21. Patients who are determined to be in severe pain from other concomitant conditions
Exclusion criteria
1. patients \<18 and \>80 2. any patient who does not meet the inclusion criteria listed for this study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postoperative change in pain and change the need for opiates after total knee arthroplasty. | 14 days | opioid consumption after surgery will be calculated in morphine equivalents |
Countries
United States
Outcome results
None listed