ADOPT PGx is a study aiming to find safe and effective drug therapies for pain and depression. It includes three trials – Acute Pain, Chronic Pain, and Depression – grouped under one protocol due to similarities in intervention, hypotheses, and trial design.
Study Overview
Status
Completed
Timeline
February 2021 – May 2024
Design
All three arms are designed as prospective, multicenter, two-arm randomized pragmatic trials to evaluate the impact of pharmacogenetic testing and genotype-guided pain or antidepressant therapy on pain control or depression symptoms.
Intervention / Treatment
Pharmacogenetic Testing
Sponsor
National Human Genome Research Institute (NHGRI)
QUICK LINKS
ACUTE PAIN
To assess whether using genotype-guided therapy for acute pain after surgery improves pain control compared to standard care, measured by a reduction in pain scores using the Silverman Integrated Approach (SIA). For more information about the acute pain trial, visit the ClinicalTrials.gov page: Acute Pain Trial.
PARTICIPATION CRITERIA
- At least 8 years of age or older
- English or Spanish speaking
- Planned or anticipated treatment with tramadol, hydrocodone, or codeine for pain relief after an elective surgery type at an enrolling site (i.e. orthopedic surgeries, open abdominal surgery, cardiothoracic surgery, etc.)
PRINCIPAL INVESTIGATORS
- Larisa Cavallari, PharmD
Dean and Distinguished Professor
College of Pharmacy
University of Florida
- Julie Johnson, PharmD
Professor of Medicine and Pharmacy
Director, Clinical and Translational Science Institute
Associate Dean, Clinical and Translational Science
Associate Vice President for Research
The Ohio State University
CHRONIC PAIN
To assess using genotype-guided pain therapy in individuals with at least three months of chronic pain improves pain control compared to standard care.
For more information about the chronic pain trial, visit the ClinicalTrials.gov page: Chronic Pain Trial.
PARTICIPATION CRITERIA
- At least 18 years of age or older
- English or Spanish speaking
- History of pain for at least 3 months
- Seen at primary care or pain-relevant specialty clinics
- Currently treated or being considered for treatment with tramadol, hydrocodone, or codeine for pain relief
PRINCIPAL INVESTIGATORS
- Todd Skaar, PhD
Professor of Medicine
Division of Clinical Pharmacology
Indiana University School of Medicine
- Paul Dexter, MD
Associate Professor of Clinical Medicine
Division of General Internal Medicine
Indiana University School of Medicine
DEPRESSION
To assess using genetic guidance to dose or select antidepressants in individuals with at least three months of depressive symptoms, who need new or adjusted antidepressant therapy, improves depression management compared to standard care. For more information about the depression trial, visit the ClinicalTrials.gov page: Depression Trial.
PARTICIPATION CRITERIA
- At least 8 years of age or older
- English or Spanish speaking
- Patients followed at psychiatry or primary care clinics at an enrolling site
- Documentation of depression and/or provider report of depression
- Evidence of depressive symptoms for at least 3 months based on patient interview or documentation in patient's medical records
- Recent initiation of SSRI therapy, revised SSRI therapy, or anticipated need for revised or new SSRI therapy per healthcare provider
PRINICIPAL INVESTIGATORS
- Josh F. Peterson, MD, MPH
Professor of Biomedical Informatics and Medicine
Vanderbilt University
- Kerri L. Cavanaugh, MD, MHS
Associate Professor of Medicine
Division of Nephrology and Hypertension
Vanderbilt University
