This project consists of a randomized controlled study design. Study candidates will include all patients 18 years or older, who were evaluated at UCSD and found to have an orthopaedic injury requiring surgery. Patients who consent to study participation will be randomized to receive either the multimodal pain management protocol or standard oral hydrocodone-acetaminophen for post-operative pain management. Data on opioid usage, pain control, and functional status will be collected for each participant. After 3 years of data collection, investigators will analyze this data to provide further insight in determining appropriateness of pain regimens that reduce the overall opioid consumption. Given the widespread opioid epidemic, it is imperative to develop alternative means to appropriately manage pain in orthopaedic surgery patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Multimodal Pain Management to minimize patients' reliance on opioids.
University of California, San Diego
San Diego, California, United States
Morphine equivalents used
Morphine equivalents used over 1 year
Time frame: 1 year
Pain Score (0-10, 0=no pain, 10=most severe pain)
Time frame: 1 year
Number of Complications
Time frame: 1 year
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