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Nonopioid Analgesia After Labral Surgery

RecruitingPhase 2, Phase 3Ages 18 Years - anyAllHenry Ford Health System
NCT03825809 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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

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📋 Eligibility rules (as published)
Eligibility Criteria: Inclusion Criteria: * All adult patients over age 18 and scheduled for a primary or revision labral surgery Exclusion Criteria: * 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
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What it tests

  • Celecoxib
  • Hydrocodone-Acetaminophen
  • Ketorolac
  • Gabapentin
  • Acetaminophen
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Where

1 site
Henry Ford Health System
Detroit, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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