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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Oral cannabis (placebo) | Placebo Comparator | Participants will receive placebo oral cannnabis |
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| Oral cannabis (active) | Experimental | Participants will receive active oral cannabis |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Inhaled Cannabis | Drug | Participants will receive inhaled cannabis and placebo |
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| Measure | Description | Time Frame |
|---|---|---|
| Opioid withdrawal severity | Opioid severity is a participant-rated outcome that will be measured on a visual analog scale (0-100) | This outcome will be assessed regularly from baseline through 6 hours post cannabis dose during experimental sessions. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Paul Nuzzo | Contact | 859-323-0002 | paul.nuzzo@uky.edu |
| Name | Affiliation | Role |
|---|---|---|
| Shanna Babalonis, PhD | University of Kentucky College of Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Kentucky | Lexington | Kentucky | 40508 | United States |
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| ID | Term |
|---|---|
| D009293 | Opioid-Related Disorders |
| D002189 | Marijuana Abuse |
| ID | Term |
|---|---|
| D000079524 | Narcotic-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
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| Intranasal Opioid | Drug | Participants will receive intranasal opioids and placebo |
|