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Nonopioid Analgesia After Labral Surgery
Sponsor: Henry Ford Health System
Summary
This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen
Official title: Traditional vs. Nonopioid Analgesia After Labral Surgery
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
100
Start Date
2019-01-22
Completion Date
2020-05-20
Last Updated
2019-01-31
Healthy Volunteers
Yes
Conditions
Interventions
Celecoxib
Post-Operative Non Opioid Pain Protocol
Hydrocodone-Acetaminophen
Traditionally used narcotic pain protocol
Ketorolac
Post-Operative Non Opioid Pain Protocol
Gabapentin
Post-Operative Non Opioid Pain Protocol
Acetaminophen
Post-Operative Non Opioid Pain Protocol
Diazepam
Post-Operative Non Opioid Pain Protocol
Locations (1)
Henry Ford Health System
Detroit, Michigan, United States