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NCT05525923 · ClinicalTrials.gov registry record

Personalized Postoperative Pain Management Following Thoracic Surgery in Adults

A clinical trial of Thoracic Surgery and Lobectomy, sponsored by OpalGenix.

Recruiting
Registry status
200
Enrollment target
4
Study locations

NCT05525923 is a study of Thoracic Surgery and Lobectomy that is actively recruiting participants, run by OpalGenix. The registered enrollment target is 200 participants, above the 139-participant average among 5 other Thoracic Surgery trials with a reported enrollment target (44% higher). The trial reports 4 study locations across 1 state.

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The verdict

NCT05525923, a study of Thoracic Surgery and Lobectomy, is actively recruiting participants, sponsored by OpalGenix.

RECRUITING
Registry status
200 participants
Enrollment target
4
Study locations

Study 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 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.

Study Locations (4)

Pennsylvania

  • UPMC Presbyterian Hospital - Pittsburgh
  • UPMC Mercy Hospital - Pittsburgh
  • UPMC Shadyside Hospital - Pittsburgh
  • UPMC Passavant Hospital - Pittsburgh

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2023-11-30
Est. Completion 2028-03-01

Sponsor

OpalGenix

2 total trials

What the Registry Record Tells You About NCT05525923

The ClinicalTrials.gov registry entry for NCT05525923 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 139-participant average among 5 other Thoracic Surgery trials with a reported enrollment target (44% higher). The listed sponsor is OpalGenix, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Thoracic Surgery appearing as the primary indexed condition, and to 0 interventions.

NCT05525923 reports 4 study locations spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT05525923 about?

NCT05525923 is a clinical study titled "Personalized Postoperative Pain Management Following Thoracic Surgery in Adults". 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 inp...

What is the current status of trial NCT05525923?

This trial is currently recruiting. The enrollment target is 200 participants. The study started on 2023-11-30. Estimated completion is 2028-03-01.

What conditions does trial NCT05525923 study?

This clinical trial studies the following conditions: Thoracic Surgery, Lobectomy, Segmentectomy, Pneumonectomy.

Who is sponsoring clinical trial NCT05525923?

This trial is sponsored by OpalGenix, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05525923 being conducted?

This trial has 4 study locations across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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