Actively Recruiting

Age: 18Years - 99Years
All Genders
NCT05525923

Personalized Postoperative Pain Management Following Thoracic Surgery in Adults

Led by OpalGenix, Inc · Updated on 2025-05-01

200

Participants Needed

4

Research Sites

221 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Personalized Postoperative Pain Management Following Thoracic Surgery in Adults

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age greater than 18 years
  • American Society of Anesthesiologists (ASA) Physical Status 1, 2, or 3
  • Undergoing thoracic surgery including pneumonectomy, lobectomy, or segmentectomy
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Pregnant women
  • American Society of Anesthesiologists (ASA) Physical Status 4 or higher
  • Non-English speaking
  • Outpatient surgery
  • Additional surgical procedures combined with thoracic surgery
  • Significant liver or kidney dysfunction
  • Significant cardiorespiratory compromise
  • Current polysubstance use such as cocaine, marijuana, or amphetamines

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

UPMC Presbyterian Hospital

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

2

UPMC Mercy Hospital

Pittsburgh, Pennsylvania, United States, 15219

Actively Recruiting

3

UPMC Shadyside Hospital

Pittsburgh, Pennsylvania, United States, 15232

Actively Recruiting

4

UPMC Passavant Hospital

Pittsburgh, Pennsylvania, United States, 15237

Actively Recruiting

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Research Team

A

Amy Monroe, MPH, MBA

CONTACT

A

Alisha Maslanka, BS

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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