Nonopioid Analgesia After Labral Surgery
ConditionNarcotic Use
Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorHenry Ford Health System
About this trial
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 criteria
Qualifiers
All adult patients over age 18 and scheduled for a primary or revision labral surgery
Disqualifiers
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
Trial design
Treatments tested in this trial
- Celecoxib
- Hydrocodone-Acetaminophen
- Ketorolac
- Gabapentin
- Acetaminophen
- Diazepam
Treatment groups
100 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov