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Recruiting NCT06078371

Opioid-Free Pain Treatment in Trauma Patients

Trial Parameters

Condition Femoral Neck Fractures
Sponsor University of Kansas Medical Center
Study Type INTERVENTIONAL
Phase N/A
Enrollment 250
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2023-11-01
Completion 2026-10
All Conditions
Femoral Neck Fractures Intertrochanteric Fractures Femoral Shaft Fracture Distal Femur Fracture Patella Fracture Tibial Shaft Fracture with or Without Associated Fibula Fracture Ankle Fracture (bimalleolar Equivalent, Bimalleolar, or Trimalleolar) Tibial Pilon Fracture Talar Head, Neck, Body, or Process Fractures Calcaneus Fractures Lisfranc Injuries Isolated or Multiple Metatarsal Fractures Phalanx Fractures of the Foot, Single or Multiple Clavicle Fractures Proximal Humerus Fractures Humeral Shaft Fractures Distal Humerus Fractures (intra or Extra-articular) Olecranon Fractures Radial Head or Neck Fractures Elbow Fractures Involving a Combination of Fractures of the Radius and Uln Forearm Fractures (both Bone Forearm Fractures, Isolated Ulnar Shaft, Isolated Radial Shaft) Distal Radius Fractures
Interventions
Opioid-free pain treatment

Brief Summary

Analgesic drug study that will compare pain outcomes of opioid analgesia and opioid-free analgesia in post-operative orthopedic patients.

Eligibility Criteria

Inclusion Criteria: * Patient is over the age of 18 years old * Underwent surgical treatment for the injuries of interest (stated elsewhere) by an Orthopedic Traumatology Attending Physician at the University of Kansas Hospital Exclusion Criteria: * Patients that are unable to provide informed consent due to sustaining a head injury or incoherence from narcotics given to them post-injury * Chronic opioid use * Under the age of 18 years old * Undergoing revision surgery * Did not undergo surgical fixation * Pregnant/nursing women * Vulnerable populations as defined by the University of Kansas Medical Center IRB * Did not experience one of the following fractures listed in D.1. above. * Patients with CKD and/or cirrhosis will be excluded from the opioid-free pain block (block 2) and will only qualify for the standard of care opioid group (Block 1)

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