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Opioid-Free Pain Protocol After Shoulder Arthroplasty
Sponsor: Henry Ford Health System
Summary
This randomized, single blinded, clinical trial aims to investigate the efficacy of a multimodal pain control regimen for shoulder arthroplasty. Patients who receive a multimodal pain control regimen alone (study group) will be compared to patients who receive a multimodal pain control regimen plus a standard prescription of an opioid containing medication (comparison group). The primary outcome is average daily Numerical Rating Scale (NRS) pain score in the first 10 days after surgery. We hypothesize that there will be no significant difference in the primary outcome between the two groups.
Official title: Multimodal Nonopioid Pain Protocol Following Shoulder Arthroplasty Surgery
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
83
Start Date
2022-06-25
Completion Date
2026-09-01
Last Updated
2026-02-10
Healthy Volunteers
Yes
Conditions
Interventions
Celecoxib
preoperative pain medication given to all patients
Pregabalin
preoperative and discharge pain medication given to all patients
Tramadol
preoperative pain medication given to all patients
Dexamethasone
Intraoperative and discharge pain medication given to all patients
Acetaminophen
Intraoperative and discharge pain medication given to all patients
Ropivicaine
Intraoperative pain medication given to all patients
Epinephrine
Intraoperative pain medication given to all patients
Ketorolac
Intraoperative pain medication given to all patients
Tizanidine
Discharge pain medication given to all patients
Magnesium
Discharge pain medication given to all patients
Ibuprofen
Discharge pain medication given to all patients
Oxycodone Hydrochloride 5 Mg
Only given to active comparator group
Locations (1)
Henry Ford Health
Detroit, Michigan, United States