Characterization of CB1 Receptors Using [11-C]OMAR in Opioid Use Disorder
Yale University · with National Institute on Drug Abuse (NIDA) · NCT07800520
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 25–65 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 110
- US sites recruiting
- 1
- Study start
- October 1, 2026
- Record last updated
- October 2, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: [11C]OMAR
Conditions: Opioid Use Disorder; OAT
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
All
- Normal screening bloodwork.
- Adequate arterial access for placement of an arterial line and blood sampling per study protocol.
OUD Participants
- Diagnosis of opioid use disorder (OUD) according to DSM-5 criteria.
- Actively seeking treatment for OUD.
- Willingness to initiate opioid agonist therapy (OAT) with buprenorphine.
Healthy Controls
- Good general physical health.
- No current or past diagnosis of any psychiatric or substance use disorders.
Exclusion Criteria
All
- Any current major medical condition that, in the opinion of the Principal Investigator, poses a risk for PET procedures.
- Prior participation in research studies within the past year that would result in cumulative radiation exposure exceeding annual limits.
- Presence of ferromagnetic metal in the body, pacemaker, or other contraindications to MRI.
- Positive pregnancy test or current lactation.
- History of neurological conditions, including stroke or seizure disorders.
- Hematocrit values lower than 30
OUD Participants
- Current or past diagnosis of a serious psychiatric disorder.
- Current diagnosis of any substance use disorder other than nicotine or opioids.
- Use of any substances within the past 30 days.
- Current use of SSRIs or benzodiazepines or use within the past 30 days.
- Previous enrollment in the main study.
Healthy Controls
- Current or past diagnosis of any psychiatric disorder.
- Current diagnosis of any substance use disorder (excluding nicotine).
- Use of any substances within the past 30 days.
Recruiting US locations
Connecticut Mental Health Center, Clinical Neuroscience Research Unit
New Haven, CT 06519
Site contact: Abigail Dewey · 475-441-4190 · abigail.dewey@yale.edu
Study contacts (from the official record)
- Anahita Bassir Nia, MD · 203-974-7540 · anahita.bassirnia@yale.edu
- Abigail Dewey · 475-441-4190 · abigail.dewey@yale.edu
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