Nonopioid Analgesia After Labral Surgery
Traditional vs. Nonopioid Analgesia After Labral Surgery
Henry Ford Health System
100 participants
Jan 22, 2019
INTERVENTIONAL
Conditions
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
Eligibility
Inclusion Criteria2
- Eligibility Criteria:
- All adult patients over age 18 and scheduled for a primary or revision labral surgery
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Interventions
Post-Operative Non Opioid Pain Protocol
Traditionally used narcotic pain protocol
Post-Operative Non Opioid Pain Protocol
Post-Operative Non Opioid Pain Protocol
Post-Operative Non Opioid Pain Protocol
Post-Operative Non Opioid Pain Protocol
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT03825809