Characterization of CB1 Receptors Using [11-C]OMAR in Opioid Use Disorder
Part of paid clinical trials in New Haven, Connecticut.
- Sponsor
- Yale University
- Study ID
- NCT07800520
- Phase
- PHASE1
- Status
- Not Yet Recruiting
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Conditions
- OAT
- Opioid Use Disorder
Eligibility Criteria
- Sex
- ALL
- Age
- 25 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- [11C]OMAR — DRUGFor each \[11C\]OMAR PET scan, up to 20 mCi of \[11C\]OMAR will be administered.
Study Details
The goals of this sub-study is to assess CB1R availability in early abstinent individuals with OUD (following opioid agonist therapy - OAT stabilization) and in matched healthy controls.
Key Dates
- First listed
- Sep 2, 2026
- Start date
- Sep 30, 2026
- Status verified
- Aug 2026
- Primary completion
- Aug 31, 2030
- Completion
- Aug 31, 2030
Study Design
- Enrollment
- 110 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- DIAGNOSTIC
Arms
- Other: Healthy VolunteersHealthy volunteers with no current or past major medical or psychiatric history
- Other: Opioid Use Disorder in Opioid Agonist Therapy (OAT)Patients diagnosed with opioid use disorder during the early phase of opioid agonist therapy
Primary Outcome Measure
CB1R Availability [ Time Frame: Day 7 ]
Central Contacts
- Anahita Bassir Nia, MD203-974-7540
- Abigail Dewey475-441-4190
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Connecticut Mental Health Center, Clinical Neuroscience Research Unit | New Haven | Connecticut | 06519 | Anahita Bassir Nia, MD (PRINCIPAL_INVESTIGATOR) |
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