Pharmacogenetics and Pharmacokinetics of Oxycodone to Personalize Postoperative Pain Management Following Lumbar Spinal Fusion and Decompression Surgery in Adults

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

The proposed research is an important extension of an ongoing perioperative personalized analgesia and intravenous opioid pharmacogenetic research. This research focuses on two of the most commonly used oral opioid analgesics, oxycodone, and methadone, in adults following lumbar spinal fusion and decompression surgery. Genetic signature and combinatorial pharmacogenetic approaches perform better than single-gene associations. This innovative translational research will for the first time evaluate simultaneously the effects of multiple genes and interactions on oxycodone and methadone's pharmacokinetics and optimal clinical dosing and on its safety and efficacy in the highly vulnerable pediatric population. This research's multigenetic signature findings can be easily extrapolated to adults undergoing surgery or using oxycodone and/or methadone for chronic and cancer pain and in identifying opioid abusers at risk of severe respiratory depression and death. When methadone is given in addition to oxycodone for inpatient pectus excavatum repair and idiopathic scoliosis spinal fusions according to new departmental protocols, methadone pharmacokinetics and pharmacodynamics will also be evaluated.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

• \>18 years of age

• American Society of Anesthesiologists (ASA) Physical Status 1, 2, or 3

• Undergoing lumbar spine surgeries (lumbar spine decompression, multilevel posterior spine fusion, internal fixation or a combination) for degenerative lumbar spine and lumbar spinal stenosis and requiring opioids for perioperative pain management

Locations
United States
Pennsylvania
UPMC Montefiore Hospital
RECRUITING
Pittsburgh
UPMC Pain Medicine at Centre Commons
RECRUITING
Pittsburgh
UPMC Presbyterian Hospital
RECRUITING
Pittsburgh
Contact Information
Primary
Amy Monroe, MPH, MBA
monroeal@upmc.edu
412-623-6382
Backup
Alisha Maslanka, BS
maslankaa@upmc.edu
412-864-6779
Time Frame
Start Date: 2022-11-01
Estimated Completion Date: 2027-07-01
Participants
Target number of participants: 235
Sponsors
Leads: OpalGenix, Inc

This content was sourced from clinicaltrials.gov