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The purpose of this study is to evaluate whether liposomal bupivacaine is superior to normal bupivacaine in terms of providing better pain control postoperatively after total knee arthroplasty.
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Lead Sponsor
University of Miami
NCT06527664 · Bone Loss, Hip Prosthesis Infection, and more
NCT05981105 · Chronic Pain, Opioid Use, and more
NCT07151443 · Peripheral Nerve Block, Pain Management, and more
NCT05845021 · Osteoporosis, Arthroplasty Complications, and more
NCT06969222 · Knee Arthropathy, Arthroplasty Complications, and more
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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