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Study identifier: NCT05525923 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Personalized Postoperative Pain Management Following Thoracic Surgery in Adults

Condition: Thoracic Surgery · Pneumonectomy · Lobectomy  ·  Sponsor: OpalGenix, Inc

PhaseN/A
Planned participants200
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

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 thoracic surgery. Major inpatient thoracic surgeries (TS) for lung disease are common and extremely painful surgeries and are associated with sever post-surgical pain, high incidence of chronic post-surgical pain (CPSP), excess opioid use, costly immediate postoperative opioid adverse events (AEs), and long hospital stays. This study is aiming to develop proactive risk prediction algorithms for precision surgical pain relief in adult TS patients through comparison of actual clinical outcomes with standard of care to predicted outcomes based on personalized risk assessments.

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

Talk to the study team

Amy Monroe, MPH, MBA  ·  412-623-6382  ·  monroeal@upmc.edu

Alisha Maslanka, BS  ·  412-864-6779  ·  maslankaaa@upmc.edu

Always discuss trial participation with your own doctor first.

Locations (4)

UPMC Presbyterian HospitalPittsburgh, Pennsylvania, United StatesRecruiting
UPMC Mercy HospitalPittsburgh, Pennsylvania, United StatesRecruiting
UPMC Shadyside HospitalPittsburgh, Pennsylvania, United StatesRecruiting
UPMC Passavant HospitalPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05525923