Thoracic SurgeryNCT05525923
Personalized Postoperative Pain Management Following Thoracic Surgery in Adults
An observational study of Thoracic Surgery and Pneumonectomy, run by OpalGenix, Inc at 4 sites in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 99 years
- Conditions the study is for
- Thoracic Surgery, Pneumonectomy, Lobectomy
- How many people
- 200 participants
- Where
- 4 sitesUnited States
- Study dates
- 30 Nov 2023to 1 Mar 2028
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 99 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Study population will be adults undergoing thoracic surgeries that fit the inclusion criteria. Children will not be included as they are not seen at the specific site institution. Given the nature of the surgical procedure, pregnant women and women that may be pregnant will also not be included in this study population.
Who may be able to join
- >18 years
- American Society of Anesthesiologists (ASA) Physical Status 1, 2, 3
- Undergoing thoracic surgery (TS; pneumonectomy, lobectomy and segmentectomy)
Who cannot join
- Children (<18 years)
- Pregnant women
- American Society of Anesthesiologists (ASA) Physical Status 4 or above
- Non-English speaking
- Outpatient surgery
- Concomitant additional surgical procedures
Show all 9Show fewer
- Significant liver and kidney dysfunction
- Significant cardiorespiratory compromise
- Patients with polysubstance use (e.g., cocaine, marijuana, amphetamine, etc.)
Trial locations and contacts
4 sites in 1 country. Contact the study team or a site near you to ask about taking part.
United States4 sites, 4 recruiting
- Recruiting
UPMC Presbyterian Hospital
Pittsburgh, Pennsylvania, 15213
Kathirvel Subramaniam, MD, MPH, subramaniamk@upmc.edu
Amy Monroe, MPH, MBA, 412-623-6382, monroeal@upmc.edu
- Recruiting
UPMC Mercy Hospital
Pittsburgh, Pennsylvania, 15219
Kathirvel Subramaniam, MD, subramaniamk@upmc.edu
Amy Monroe, MPH, MBA, 412-623-6382, monroeal@upmc.edu
- Recruiting
UPMC Shadyside Hospital
Pittsburgh, Pennsylvania, 15232
Kathirvel Subramaniam, MD, subramaniamk@upmc.edu
Amy Monroe, MPH, MBA, 412-623-6382, monroeal@upmc.edu
- Recruiting
UPMC Passavant Hospital
Pittsburgh, Pennsylvania, 15237
Kathirvel Subramaniam, MD, subramaniamk@upmc.edu
Amy Monroe, MPH, MBA, 412-623-6382, monroeal@upmc.edu
About this study
Official title: Pharmacogenetics and Pharmacokinetics of Oxycodone to Personalize 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 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.
Read the detailed description
Risks associated with post-TS pain and opioids. Opioids are still widely used to manage acute surgical pain and remain a core component of enhanced recovery after surgery protocols (ERAS) for painful TS. With current approaches that incorporate ERAS protocols, half of TS patients still suffer from uncontrolled severe surgical pain and significant adverse opioid effects due to opioids' narrow therapeutic indices and unpredictable inter-individual variations in pain perception and opioid responses. Risks associated with perioperative opioid use include immediate risks (life-threatening respiratory depression (RD), excessive sedation, postoperative nausea and vomiting (PONV), urinary retention, constipation, ileus and itching) frequently delay recovery, require additional treatment or monitoring, increase cost of care, and prolong hospital stay. Long-term risks include CPSP, opioid dependence, OUD, and the consequent personal, financial and societal burden of opioid epidemic. Post-TS CPSP: A 10% increase in the percentage of time in severe pain on the first postoperative day was associated with a 30% increase in the incidence of CPSP at 12 months (N=889), post-thoracotomy pain and TS are associated with the highest risk for CPSP compared with all other procedures. Effective and aggressive acute surgical pain management is critical to lower risks of developing CPSP.
Opioids are still an important part of managing surgical pain following TS. Postoperative pain following TS is often excruciating and challenging to treat as it provokes nociceptive, neuropathic and spasmodic muscle pain. Current standardized ERAS multimodal analgesic approaches include non-opioid analgesics to minimize opioids during and after surgery. While ERAS protocols have reduced immediate perioperative opioid use, they follow a "one size fits all" trial-and-error reactive standardized practice, and at risk patients continue to experience uncontrolled pain, CPSP, costly opioid AEs and persistent opioid use.
High inter-individual variations in response to opioids can be explained by genetics, yet translational barriers prevent widespread adoption of genotype-guided care: Our many studies on genetic predictors of postoperative pain and opioid-related AEs, and published literature from other researchers demonstrate that genetic and clinical factors are associated with inter-individual variations in surgical pain and opioid AEs. Personalized care based on validated and actionable polygenic and modifiable clinical risk factors (e.g., anxiety, depression, catastrophizing, poorly controlled acute postoperative pain) can transform and enhance post-TS pain and opioid management. Thus, there is an urgent and unmet need for a highly reliable preoperative tool to predict and prevent severe pain, CPSP and opioid-related AEs.
Inadequate acute postoperative pain management predisposes patients to the development of CPSP and contributes to opioid dependence (OD), opioid misuse, and loss of productivity in society. Opioids are continued after discharge in 76.4% of patients, with a median discharge prescription of 150 mg oral morphine equivalents. More than a third of thoracic surgical patients develop CPSP at 3 months after surgery and poor postoperative pain control predicts both incidence and severity of CPSP. Patients who develop CPSP have a high life-long risk of opioid use and misuse contributing to addiction, and overdose deaths.
Poorly controlled surgical pain, excessive opioid use, and CPSP lead to postoperative neurocognitive disorders including delirium, postoperative cognitive dysfunction (POCD), and dementia. Delirium is detected during hospitalization and neurocognitive decline lasting longer (>30 days) is described as POCD. Untreated pain and excessive perioperative opioids increase the risk of delirium and POCD in elderly individuals. A population-level Health and Retirement study of 10,065 patients >62 years old showed CPSP is common and was associated with accelerated memory decline and increased probability of dementia.
Both poorly controlled pain and excess opioid use predispose elderly surgical patients to postoperative delirium, POCD and dementia. New persistent opioid use is a significant public health problem in elderly surgical patients.
The OpalGenix Solution: GPS-Analgesics. As a Global Positioning System (GPS) helps chart a course in unknown/unfamiliar terrain, GPS-Analgesics TM (Genotype-guided Physician Support for Analgesics Use) is designed to support physicians to proactively identify patients genetically predisposed to high risks for severe surgical pain, CPSP and opioid AEs. In this Phase I proposal, OpalGenix will build on our prior studies to develop and validate GPS-Analgesics in TS patients. We have extensively and prospectively studied ~2000 patients undergoing painful surgeries and demonstrated that the high individual variation observed in responses to surgical pain and opioids can be explained by a combination of polygenetic and clinical factors. Specifically, inter-individual surgical pain, and opioid variability were partly and independently explained by specific polymorphisms of the genes ABCB123, OPRM143, CYP2B6110, ABCC351,52, FAAH22, COMT53 and OCT151. However, these single-gene associations independently explain only a small (5-15%) portion of inter-individual variability in pain- and opioid responses. GPS-Analgesics is a novel combinatorial pharmacogenetic polygenetic tool with high accuracy (>90%) integrating clinical risk factors to better explain the cumulative effects (>90%) of both polygenetic (50-60%) and clinical (40-50%) risk factors on surgical pain and analgesics responses. OpalGenix's novel prototype predictive software algorithm based on patented polygenic risks already has >80% predictivity. At the end of this Phase I, GPS-Analgesics will provide >90% high accuracy, evidence-based, personalized surgical pain while avoiding opioid-related AEs.
- Conditions
- Thoracic Surgery, Pneumonectomy, Lobectomy, Segmentectomy
- Keywords
- Pain Management, Opioid Use
- Medical subject headings
- Agnosia
What is being measured
The primary outcome is the main question the study is designed to answer.
Opioid-related Post-operative nausea and vomiting (PONV)
PONV is measured with a binary yes/no response
Measured: Post-operative up to 12 months
Opioid-related sedation
Sedation will be measured using the Riker Sedation Scale. The minimum score of 1 categorizes the patient as being unarousable, while the maximum score of 7 categorizes the patient as being dangerous agitation.
Measured: Post-operative up to 12 months
Opioid-related respiratory depression (RD)
Respiratory depression is defined as abnormally slow respiratory rate which is below 12 breaths per minute. This will be measured with a binary yes/no response pulled from the electronic medical records.
Measured: Post-operative up to 12 months
Secondary outcomes (7)
Opioid use
Inpatient total opioid usage
Measured: Pre-operative to post-operative up to 12-months
Post-operative Pain Scores
Pain scores will be measured using the patient-reported Numerical Rating Scale (NRS), in which a minimum score of 0 indicates no pain at all and a maximum score of 10 indicates the worst pain imaginable
Measured: Pre-operative to post-operative up to 12-months
Length of Hospital Stay
Length of hospital stay will be recorded as the number of days a patient remained in the hospital post-operatively
Measured: Post-operative day 1 up to 1-month
Chronic Post-surgical Pain (CPSP)
CPSP is defined as pain that develops after surgical invention and lasts at least 2 months. CPSP will be scored as yes/no.
Measured: Post-operative up to 12 months
Length of Prescribed Opioid Usage
Length of prescribed opioid usage will be recorded as the number of days patient has an active prescription which will be obtained from electronic medical records
Measured: Post-operative up to 12-months
Opioid Dependence (OD)
OD and OUD risk will be measured using the Current Opioid Misuse Measure (COMM) tool. The COMM is a 17-item questionnaire in which a score of 9 or higher is considered a positive screen for opioid misuse. Minimum score is 0 and maximum score is 68.
Measured: Post-operative up to 12 months
Opioid Use Disorder (OUD) Risk
OD and OUD risk will be measured using the Current Opioid Misuse Measure (COMM) tool. The COMM is a 17-item questionnaire in which a score of 9 or higher is considered a positive screen for opioid misuse. Minimum score is 0 and maximum score is 68.
Measured: Post-operative at 3-months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Sep 2022
- Study start30 Nov 2023
- Primary completion1 Mar 2026 (estimated)
- Study completion1 Mar 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Thoracic SurgeryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- OpalGenix, Inc
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Kathirvel Subramaniam, MD, MPH, Principal investigator, University of Pittsburgh
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05525923
- Sponsor's protocol ID
- STUDY22070047
- Status last verified
- Apr 2025
- First submitted
- 31 Aug 2022
- Last updated
- 1 May 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 May 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pharmacogenetics and Pharmacokinetics of Oxycodone to Personalize Postoperative Pain Management Following Thoracic Surgery in Adults
- ClinicalTrials.gov ID
- NCT05525923
- Acronym / sponsor ID
- STUDY22070047
- Conditions
- Thoracic Surgery, Pneumonectomy, Lobectomy, Segmentectomy
- Keywords
- Pain Management, Opioid Use
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- OpalGenix, IncIndustry (pharma, biotech, devices)
- Study start
- 30 Nov 2023 (actual)
- Primary completion
- 1 Mar 2026 (estimated)
- Study completion
- 1 Mar 2028 (estimated)
- First posted
- 2 Sep 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Risks associated with post-TS pain and opioids. Opioids are still widely used to manage acute surgical pain and remain a core component of enhanced recovery after surgery protocols (ERAS) for painful TS. With current approaches that incorporate ERAS protocols, half of TS patients still suffer from uncontrolled severe surgical pain and significant adverse opioid effects due to opioids' narrow therapeutic indices and unpredictable inter-individual variations in pain perception and opioid responses. Risks associated with perioperative opioid use include immediate risks (life-threatening respiratory depression (RD), excessive sedation, postoperative nausea and vomiting (PONV), urinary retention, constipation, ileus and itching) frequently delay recovery, require additional treatment or monitoring, increase cost of care, and prolong hospital stay. Long-term risks include CPSP, opioid dependence, OUD, and the consequent personal, financial and societal burden of opioid epidemic. Post-TS CPSP: A 10% increase in the percentage of time in severe pain on the first postoperative day was associated with a 30% increase in the incidence of CPSP at 12 months (N=889), post-thoracotomy pain and TS are associated with the highest risk for CPSP compared with all other procedures. Effective and aggressive acute surgical pain management is critical to lower risks of developing CPSP.
Opioids are still an important part of managing surgical pain following TS. Postoperative pain following TS is often excruciating and challenging to treat as it provokes nociceptive, neuropathic and spasmodic muscle pain. Current standardized ERAS multimodal analgesic approaches include non-opioid analgesics to minimize opioids during and after surgery. While ERAS protocols have reduced immediate perioperative opioid use, they follow a "one size fits all" trial-and-error reactive standardized practice, and at risk patients continue to experience uncontrolled pain, CPSP, costly opioid AEs and persistent opioid use.
High inter-individual variations in response to opioids can be explained by genetics, yet translational barriers prevent widespread adoption of genotype-guided care: Our many studies on genetic predictors of postoperative pain and opioid-related AEs, and published literature from other researchers demonstrate that genetic and clinical factors are associated with inter-individual variations in surgical pain and opioid AEs. Personalized care based on validated and actionable polygenic and modifiable clinical risk factors (e.g., anxiety, depression, catastrophizing, poorly controlled acute postoperative pain) can transform and enhance post-TS pain and opioid management. Thus, there is an urgent and unmet need for a highly reliable preoperative tool to predict and prevent severe pain, CPSP and opioid-related AEs.
Inadequate acute postoperative pain management predisposes patients to the development of CPSP and contributes to opioid dependence (OD), opioid misuse, and loss of productivity in society. Opioids are continued after discharge in 76.4% of patients, with a median discharge prescription of 150 mg oral morphine equivalents. More than a third of thoracic surgical patients develop CPSP at 3 months after surgery and poor postoperative pain control predicts both incidence and severity of CPSP. Patients who develop CPSP have a high life-long risk of opioid use and misuse contributing to addiction, and overdose deaths.
Poorly controlled surgical pain, excessive opioid use, and CPSP lead to postoperative neurocognitive disorders including delirium, postoperative cognitive dysfunction (POCD), and dementia. Delirium is detected during hospitalization and neurocognitive decline lasting longer (>30 days) is described as POCD. Untreated pain and excessive perioperative opioids increase the risk of delirium and POCD in elderly individuals. A population-level Health and Retirement study of 10,065 patients >62 years old showed CPSP is common and was associated with accelerated memory decline and increased probability of dementia.
Both poorly controlled pain and excess opioid use predispose elderly surgical patients to postoperative delirium, POCD and dementia. New persistent opioid use is a significant public health problem in elderly surgical patients.
The OpalGenix Solution: GPS-Analgesics. As a Global Positioning System (GPS) helps chart a course in unknown/unfamiliar terrain, GPS-Analgesics TM (Genotype-guided Physician Support for Analgesics Use) is designed to support physicians to proactively identify patients genetically predisposed to high risks for severe surgical pain, CPSP and opioid AEs. In this Phase I proposal, OpalGenix will build on our prior studies to develop and validate GPS-Analgesics in TS patients. We have extensively and prospectively studied ~2000 patients undergoing painful surgeries and demonstrated that the high individual variation observed in responses to surgical pain and opioids can be explained by a combination of polygenetic and clinical factors. Specifically, inter-individual surgical pain, and opioid variability were partly and independently explained by specific polymorphisms of the genes ABCB123, OPRM143, CYP2B6110, ABCC351,52, FAAH22, COMT53 and OCT151. However, these single-gene associations independently explain only a small (5-15%) portion of inter-individual variability in pain- and opioid responses. GPS-Analgesics is a novel combinatorial pharmacogenetic polygenetic tool with high accuracy (>90%) integrating clinical risk factors to better explain the cumulative effects (>90%) of both polygenetic (50-60%) and clinical (40-50%) risk factors on surgical pain and analgesics responses. OpalGenix's novel prototype predictive software algorithm based on patented polygenic risks already has >80% predictivity. At the end of this Phase I, GPS-Analgesics will provide >90% high accuracy, evidence-based, personalized surgical pain while avoiding opioid-related AEs.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 99 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Study population will be adults undergoing thoracic surgeries that fit the inclusion criteria. Children will not be included as they are not seen at the specific site institution. Given the nature of the surgical procedure, pregnant women and women that may be pregnant will also not be included in this study population.
Key inclusion criteria (3 listed)
- >18 years
- American Society of Anesthesiologists (ASA) Physical Status 1, 2, 3
- Undergoing thoracic surgery (TS; pneumonectomy, lobectomy and segmentectomy)
Key exclusion criteria (9 listed)
- Children (<18 years)
- Pregnant women
- American Society of Anesthesiologists (ASA) Physical Status 4 or above
- Non-English speaking
- Outpatient surgery
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Opioid-related Post-operative nausea and vomiting (PONV)
Time frame: Post-operative up to 12 months
PONV is measured with a binary yes/no response
Opioid-related sedation
Time frame: Post-operative up to 12 months
Sedation will be measured using the Riker Sedation Scale. The minimum score of 1 categorizes the patient as being unarousable, while the maximum score of 7 categorizes the patient as being dangerous agitation.
Opioid-related respiratory depression (RD)
Time frame: Post-operative up to 12 months
Respiratory depression is defined as abnormally slow respiratory rate which is below 12 breaths per minute. This will be measured with a binary yes/no response pulled from the electronic medical records.
7 secondary outcomes
Opioid use
Time frame: Pre-operative to post-operative up to 12-months
Post-operative Pain Scores
Time frame: Pre-operative to post-operative up to 12-months
Length of Hospital Stay
Time frame: Post-operative day 1 up to 1-month
Chronic Post-surgical Pain (CPSP)
Time frame: Post-operative up to 12 months
Length of Prescribed Opioid Usage
Time frame: Post-operative up to 12-months
Opioid Dependence (OD)
Time frame: Post-operative up to 12 months
Opioid Use Disorder (OUD) Risk
Time frame: Post-operative at 3-months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 May 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Kathirvel Subramaniam, MD, MPH principal investigator
University of Pittsburgh
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Thoracic Surgery and Pneumonectomy, run by OpalGenix, Inc at 4 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 1 May 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Amy Monroe, MPH, MBA (412-623-6382, monroeal@upmc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Opioid-related Post-operative nausea and vomiting (PONV) (time frame: Post-operative up to 12 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 May 2025.