Transition From Acute to Chronic Opioid Use and Chronic Pain
NCT07211399 · Status: NOT_YET_RECRUITING · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 700
Last updated 2026-04-28
Summary
In the current opioid crisis, the use of opioids as the main pain management method is recognized as a consistent risk factor for chronic opioid use and the development of Opioid Use Disorder (OUD), as well as related complications like overdose fatalities among surgical patients. The most recent data suggests that 3.1%-10.5% of surgical patients are at risk of developing OUD. On average, there are over 40 million major surgeries that require post-op pain management, taking place in the United States each year. This puts over 1 million American surgical patients at risk for opioid dependency and misuse.
This is a prospective randomized controlled intervention study that will examine the physical and emotional outcomes of surgical patients who receive intraoperative Opioid-Free Anesthesia (OFA) supplemented with Non-Opioid Analgesia (NOAs), and how this relates to surgical patients who receive intraoperative Opioid-Based Anesthesia (OBA).
Conditions
Interventions
- DRUG
-
Opioid-free anesthesia
Each patient will be pre-oxygenated receive IV-acetaminophen (1 g), and IV-lidocaine (60 - 100 mg). and dexmedetomidine (12-20 mcg IV) and ketamine (25-50 mcg) prior to intubation. Induction of anesthesia will be achieved with IV-propofol (1 - 2 mg/kg; 150 - 200 mg). Patient air ways will be secured with an intratracheal tube or LMA. Anesthesia will be maintained by either propofol (100 - 150 mcg/kg/hour; TIVA), or sevoflurane (0.5-1 MAC). During surgery, dexmedetomidine and ketamine will be administered as needed. Anesthesia will be maintained by either propofol (100 - 150 mcg/kg/hour; TIVA), or sevoflurane (0.5-1 MAC).
- DRUG
-
Opioid-based anesthesia
Each patient will be pre-oxygenated receive IV-acetaminophen (1 g), and IV-lidocaine (60 - 100 mg). and fentanyl 50-100 mcg IV prior to intubation. Induction of anesthesia will be achieved with IV-propofol (1 - 2 mg/kg; 150 - 200 mg). Patient air ways will be secured with an intratracheal tube or LMA. Anesthesia will be maintained by either propofol (100 - 150 mcg/kg/hour; TIVA), or sevoflurane (0.5-1 MAC). During surgery, each patient in the opioid group will receive IV-fentanyl (50 - 100 mcg) as needed.
Sponsors & Collaborators
-
Jacques E. Chelly
lead OTHER
Principal Investigators
-
Jacques Chelly, MD, PhD, MBA · University of Pittsburgh, UPMC
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-07-01
- Primary Completion
- 2030-12-01
- Completion
- 2030-12-01
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Opioid Consumption After Orthopaedic Surgery
NCT03173131 ·Status: UNKNOWN ·Phase: NA
-
Using Honest Placebos to Improve Pain Management in Hand Surgery Patients
NCT03631251 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Self-reported Usage Patterns of Opioid Analgesic Medications After Surgery
NCT03034278 ·Status: COMPLETED
-
Risk of Failed Epidural in Patients With and Without Chronic Pain and Opioid Use
NCT05662566 ·Status: COMPLETED
-
Persistent Opioid Consumption After Major Abdominal Surgery and Its Determinants
NCT05197465 ·Status: COMPLETED
-
Assessment of the Development of Postoperative Persistent Postoperative Pain
NCT05370924 ·Status: RECRUITING
-
The Prevalence of Chronic Pain and Continued Opioid Use After Cardiac Surgery
NCT03412448 ·Status: UNKNOWN
-
Opioid-free Anesthesia as an Alternative to General Anesthesia in Abdominal Surgery
NCT06380244 ·Status: RECRUITING ·Phase: NA
-
A Randomized-controlled Trial of Post-operative Opiate Quantities After Urogynecologic Surgery
NCT03319277 ·Status: COMPLETED ·Phase: NA
-
Reducing Opioid Use for Chronic Pain Patients Following Surgery
NCT03675386 ·Status: RECRUITING ·Phase: NA
-
Prediction and Characterization of Acute and Chronic Postoperative Pain
NCT01308385 ·Status: COMPLETED
-
Risk Factors for Long-term Opioid Use
NCT04928131 ·Status: COMPLETED
-
Characterization of Bio-psychosocial Pain Profiles in the Perioperative Period
NCT03081299 ·Status: COMPLETED
-
Effectiveness of an Opioid Sparing Pain Regimen in Cardiac Surgery
NCT03679013 ·Status: COMPLETED ·Phase: PHASE2
-
Predicting Chronic Pain Following Breast Surgery
NCT04967352 ·Status: UNKNOWN
-
Pilot Trial: Postoperative Opioid-free Analgesia
NCT04254679 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Pharmacokinetic, Pharmacodynamic and Pharmacogenetic of Morphine After Surgery
NCT00822549 ·Status: COMPLETED
-
Sex Hormones, Postoperative Pain and Opioid Use
NCT06023225 ·Status: RECRUITING
-
Precision Analgesia for Cardiac Surgery
NCT05612399 ·Status: NOT_YET_RECRUITING
-
Preemptive Analgesia With OxyContin Versus Placebo Before Surgery for Long Bone Fractures
NCT00254631 ·Status: COMPLETED ·Phase: PHASE4
-
Pain and Function After Orthopedic Surgery
NCT01390298 ·Status: COMPLETED
-
Oxycodone vs Fentanyl for Pain Treatment After Laparoscopic Cholecystectomy
NCT00369811 ·Status: COMPLETED ·Phase: PHASE4
-
Does Preoperative Pain Medication Management Influence Surgical Outcomes in Spinal Fusion
NCT04095624 ·Status: COMPLETED ·Phase: NA
-
Opioid Free Anesthesia: What About Patient Comfort?
NCT02882035 ·Status: COMPLETED ·Phase: PHASE4
-
Opioid-Free Pain Treatment in Trauma Patients
NCT06078371 ·Status: RECRUITING ·Phase: NA