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A non-blinded randomized controlled trial, in which participants undergoing primary reverse or total shoulder arthroplasty are randomly assigned to one of two treatment groups.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| interscalene brachial plexus block | Active Comparator | Direct interscalene nerve block injection via brachial plexus |
|
| Bupivacaine extended-release liposome injection | Active Comparator | Infiltration of local anesthetic/analgesic, Bupivacaine extended-release liposome injection (Exparel) + Diluted in 40cc of Saline into the capsule, subscapularis, deltoid, pectoralis major and subcutaneous tissues. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Interscalene brachial plexus block | Procedure |
| ||
| bupivacaine extended-release liposome injection |
| Measure | Description | Time Frame |
|---|---|---|
| Morphine and Morphine Equivalent consumption | 24 hours following surgery |
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Inclusion Criteria:
1. All individuals undergoing primary reverse and total shoulder arthroplasty by the shoulder service at Methodist Hospital or Rothman Specialty Hospital.
Exclusion Criteria:
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| Procedure |
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