Actively Recruiting
Nonopioid Analgesia After Labral Surgery
Led by Henry Ford Health System · Updated on 2019-01-31
100
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Nonopioid Analgesia After Labral Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients over age 18
- Scheduled for primary or revision labral surgery
You will not qualify if you...
- Known allergies or intolerance to Celebrex, Tylenol, Neurontin, dexamethasone, tramadol
- History of substantial alcohol or drug abuse
- Pregnancy
- Narcotic use within 6 months before surgery
- Renal impairment
- Peptic ulcer disease or gastrointestinal bleeding
- Intact rotator cuff
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Henry Ford Health System
Detroit, Michigan, United States, 48202
Actively Recruiting
Research Team
T
Toufic R Jildeh, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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