University of Kentucky
Lexington, Kentucky, 40508, United States
NCT Number: NCT07661446
This inpatient study enrolls healthy individuals who have opioid use disorder. Participants live at the University of Kentucky Hospital for approx. 6 weeks. During this time, we will examine how repeated doses of oral cannabis and acute doses of oral and inhaled cannabis 1) modify the intensity and time course of opioid withdrawal, 2) modify the effects of intranasal opioid administration and 3) impact the safety of opioid administration.
Trial opening soon.
Get Notified18 year–55 year
All sexes
Interventional
Phase 1
Lexington, Kentucky, 40508, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive inhaled cannabis and placebo
Participants will receive intranasal opioids and placebo
Time frame: This outcome will be assessed regularly from baseline through 6 hours post cannabis dose during experimental sessions.
Opioid severity is a participant-rated outcome that will be measured on a visual analog scale (0-100)
Contact information is provided by the study sponsor or research team.
University of Kentucky
Other
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