Home › Opioid Overdose › NCT07800520
Characterization of CB1 Receptors Using [11-C]OMAR in Opioid Use Disorder
RecruitingPhase 1Healthy volunteers welcome
Who can join
Ages 25 to 65 · All sexes · Healthy volunteers welcome
Full eligibility 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.
About the study
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.
What is being tested
- [11C]OMAR (drug)
Sponsor: Yale University · Participants: 110 · Started: Oct 1, 2026
Contact the study team
- Anahita Bassir Nia, MD · Phone: 203-974-7540
- Abigail Dewey · Phone: 475-441-4190
Official record on ClinicalTrials.gov — NCT07800520
Locations in the U.S.
| Connecticut | Connecticut Mental Health Center, Clinical Neuroscience Research Unit, New Haven |
Conditions
From ClinicalTrials.gov, data retrieved Oct 3, 2026. Each study sets its own eligibility; the study team decides who can join.