RecruitingNarcotic Use
Nonopioid Analgesia After Labral Surgery
Eligible age
18+ yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
Yes
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
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
Sponsor: Henry Ford Health System
You may qualify if…
- ✓ All adult patients over age 18 and scheduled for a primary or revision labral surgery
You may not qualify if…
- ✕ Exclusion criteria will include patients with a medical history of known allergies or intolerance to allergies or intolerance to Celebrex, Tylenol, Neurontin, dexamethasone, tramadol, substantial alcohol or drug abuse, and pregnancy, history of narcotics within 6 months of surgery, renal impairment, peptic ulcer disease, GI bleeding. Secondary exclusion criterion is an intact rotator cuff
Where it's recruiting
Michigan
Detroit
Source: ClinicalTrials.gov · NCT03825809 · last updated 2019-01-31