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Study identifier: NCT03825809 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Nonopioid Analgesia After Labral Surgery

Condition: Narcotic Use  ·  Sponsor: Henry Ford Health System

PhasePhase 2/Phase 3
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

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

This description comes directly from the study's public registry record.

Talk to the study team

Toufic R Jildeh, MD  ·  517-230-8511  ·  tjildeh1@hfhs.org

Always discuss trial participation with your own doctor first.

Locations (1)

Henry Ford Health SystemDetroit, Michigan, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT03825809