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Study identifier: NCT06113211 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Nonopioid Pain Control Regimen After Open Reduction and Internal Fixation of Traumatic Fractures

Condition: Opioid Use · Fractures, Bone · Trauma  ·  Sponsor: Henry Ford Health System

PhasePhase 4
Planned participants75
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

An open reduction and internal fixation is a painful procedure requiring intensive postoperative pain management. Traditionally, opioid analgesia has been the gold standard for postoperative pain control. However, given the harmful side effect profile and opioid epidemic in the United States, it is advantageous to use alternate forms of analgesia. Multimodal pain control captures the effectiveness of different analgesic modalities and maximizes analgesia while minimizing side effects. The theory behind their use is that agents with different mechanisms of action work synergistically in preventing acute pain. Objective: To measure postoperative pain control in patients in two treatment arms of ORIF of the clavicle: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen. Study Design: A randomized single blinded standard of care controlled clinical trial comparing pain management interventions. All adult patients scheduled for an ORIF following a traumatic fracture by fellowship trained Trauma surgeons will be eligible for inclusion. Patients will be excluded if their medical history presents known allergies or intolerance to Motrin, Lyrica, Tylenol, Zanaflex, substantial alcohol or drug abuse, and pregnancy, history of narcotics within 6 months of surgery, renal impairment, peptic ulcer disease, GI bleeding. On the day of surgery, patients will be randomized to receive a nonopioid pain contro…

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

Talk to the study team

William Hakeos  ·  3132055349  ·  whakeos1@hfhs.org

Always discuss trial participation with your own doctor first.

Locations (1)

Henry Ford Hospital SystemDetroit, Michigan, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06113211