The Potential of Oxytocin to Reduce Opioid Abuse Liability and Pain Among Older Adults
Start Date
9/12/2023
Completion Date
7/1/2027
Summary
Some research suggests that administration of oxytocin with oxycodone may reduce its abuse liability and improve its ability to reduce pain. In a 6-session laboratory study, we will be evaluating the effects of oxycodone and oxytocin (combined and separately, across sessions) on experimentally-induced pain, subjective effects, and decision-making.
Detailed Description
The overall project goals are to determine oxytocin effects on oxycodone's subject-rated abuse liability, and experimental pain. Generally healthy individuals (determined via medical history review and a screening session) will, after informed consent, self-administer intranasal oxytocin (or placebo, containing the same ingredients but no oxytocin) shortly after oral oxycodone or placebo in a non-residential, double-blind, randomized, placebo-controlled, within-subjects laboratory study. Prescreening will assure drug application safety and, using a validated, comprehensive pain history interview, determine previous or existing chronic pain conditions, including current pain medication use.
Eligibility Criteria
Age Range: 45 years to 85 years
Interventions
OxyCODONE 5 mg Oral Tablet
OxyCODONE 2.5 mg Oral Tablet
Placebo oxyCODONE Oral Tablet
Oxytocin Nasal Spray (48 IU)
Placebo Oxytocin Nasal Spray
Conditions
Locations
University of Florida
Gainesville, Florida 32611
United States