Condition: Chronic Pain · Opioid Use · Adductor Canal Block · Sponsor: Hospital for Special Surgery, New York
The goal of this interventional clinical trial is to assess opioid consumption 24-48 hrs post anesthesia block among patients undergoing total knee arthroplasty. The main question it aims to answer is: 1\. Is there a difference in opioid consumption 24-48 hours post block administration among patients that receive an adductor canal catheter (ACC) versus adductor canal block (ACB)? Participants will be: * Randomized to receive an adductor canal catheter (ACC) or a sham adductor canal catheter. * Asked to use the Diagnotes application to communicate with the pain doctor while the catheter is in place. * Follow up for up to 6 months post-operation. Researchers will compare the interventional group (ACC) to the control group (sham ACC + ACB) to see if there is difference in opioid consumption and chronic pain at 6 months post-operation.
This description comes directly from the study's public registry record.
Pa Thor, PhD · 646-797-8535 · thorp@hss.edu
Stavros Memtsoudis, MD/PhD · 212-606-1036 · memtsoudiss@hss.edu
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| Hospital for Special Surgery | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05981105