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Clinical Trial Summary

The purpose of this study is to compare an FDA-approved medication for post-operative pain control (HTX-011) to the standard of care institutional practice for periarticular analgesia after primary total knee arthroplasty (weight based dosing of Ropivacaine, epinephrine and ketorolac diluted with saline). We are doing this research study to find out if this new medication provides superior pain control within 72 hours following surgery.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05188053
Study type Interventional
Source Mayo Clinic
Status Enrolling by invitation
Phase Phase 4
Start date March 2022
Completion date January 2024

See also
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