Low-dose Buccal Buprenorphine: Relative Abuse Potential and Analgesia
Start Date
10/19/2023
Completion Date
2/1/2028
Summary
The goal of this study is to compare the abuse potential of low-dose equianalgesic buccal buprenorphine to a commonly used full mu opioid receptor (MOR) agonist in a highly controlled experimental setting. This is a translational study in which healthy participants are phenotyped for psychosocial and Opioid-Use-Disorder-risk-related metrics. In a within-subjects crossover design, 60 participants will receive a standard postoperative oral oxycodone dose (10 mg), placebo, and 3 different doses of buccal buprenorphine across 5 separate sessions. Quantitative Sensory Testing (QST) will be used to evaluate alterations in pain responsiveness relative to placebo across buprenorphine doses and oxycodone, and will compare abuse potential (indexed by the standard FDA drug liking metric) following equianalgesic doses of the two drugs.
Eligibility Criteria
Age Range: 18 years to 65 years
Interventions
Buccal Buprenorphine 300 mcg
Buccal Buprenorphine 600 mcg
Buccal Buprenorphine 900 mcg
Buccal Placebo
Oral Placebo
Oral immediate-release oxycodone 10mg
Buccal Buprenorphine 450mcg
Conditions
Locations
Vanderbilt University Medical Center
Nashville, Tennessee 37069
United States