RECRUITING

Opioid-Free Pain Treatment in Trauma Patients

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Peri-operative Opioid-free Analgesic Protocol for Orthopedic Trauma Patients

Quick Facts

Study Start:2023-11-01

Study Completion:2026-10

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06078371

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion 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	* 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)

Inclusion Criteria

Exclusion 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

* 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)

Contacts and Locations

Study Contact

Archie Heddings, MD

CONTACT

913-588-6164

aheddings@kumc.edu

Dave Turkowitch, BS

CONTACT

dturkowitch@kumc.edu

Study Locations (Sites)

The University of Kansas Medical Center

Kansas City, Kansas, 66103

United States

Collaborators and Investigators

Sponsor: University of Kansas Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-11-01

Study Completion Date2026-10

Study Record Updates