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Clinical Trial Summary

To compare the safety and effectiveness of two pain control pathways following routine orthopaedic surgical procedures (single level or two-level ACDF/ACDA, 1st CMC arthroplasty, Hallux Valgus/Rigidus corrections, diagnostic knee arthroscopies, total hip arthroplasty, and total shoulder arthroplasty / reverse total shoulder arthroplasty). The control group will undergo surgery with an opioid-based pain protocol and the intervention group will undergo surgery with a multimodal, opioid-free protocol. Patients will have data collected with respect to pain scores, overall comfort level, overall satisfaction with the surgical experience and recovery, constipation, falls, and overall satisfaction with pain control, in addition to procedure-specific outcome scores and patient-specific metrics.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04176783
Study type Interventional
Source OrthoCarolina Research Institute, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date March 26, 2018
Completion date December 31, 2024

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