Actively Recruiting

Age: 18Years - 55Years
MALE
Healthy Volunteers
ID01730781

Characterization of CB1 Receptors Using [11-C]OMAR PET Imaging in Males Aged 18 to 55 with Psychiatric and Substance Use Conditions

Led by Yale University · Updated on 2026-04-27

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

Y

Yale University

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the availability and distribution of cannabinoid receptors (CB1R) in the human brain across various groups including healthy individuals, those with cannabis use disorders, psychotic disorders, prodromal psychotic illness, family history of alcoholism, Post-Traumatic Stress Disorder (PTSD), and Opioid Use Disorder (OUD). The study uses Positron Emission Tomography (PET) imaging with the radioligand [11-C]OMAR to visualize these receptors and aims to expand understanding based on pilot data and evolving knowledge of cannabinoid receptor function in psychiatric conditions. Participants undergo PET scans using the radiotracer [11-C]OMAR, administered at doses not exceeding 10 micrograms at the start of each scan. Those with cannabis use disorder will have multiple scans: once while using cannabis normally, once after 48 hours of abstinence, and once after four weeks of abstinence. Some patients with schizophrenia or prodromal symptoms may also have repeated scans to assess medication effects and illness progression. The study includes groups such as schizophrenia patients (on and off medication), cannabis users, individuals with a family history of alcoholism, prodromal patients, healthy volunteers, and those with PTSD or OUD. Participants will have a PET scan typically within four weeks of screening, with additional scans depending on their group and condition. Researchers will collect imaging data to measure CB1 receptor presence and distribution. This observational study includes assessments through PET imaging and monitors participants for safety and exposure to radiation. The total participation timeframe and monitoring depend on individual group protocols, with some having repeated scans over weeks to months.

CONDITIONS

Brief Title

Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning

Who Can Participate

Age: 18Years - 55Years
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male participants aged 18 to 55 years
  • Willingness to abstain from cannabis use for four weeks (for cannabis users)
  • Diagnosis of schizophrenia or schizoaffective disorder according to DSM-IV-TR (for schizophrenia group)
  • Meeting SIPS criteria for prodromal syndrome (for prodrome group)
  • Having a first-degree relative with alcoholism (for family history group)
  • Diagnosis of Post-Traumatic Stress Disorder according to DSM-IV-TR (for PTSD group)
  • Diagnosis of Opioid Use Disorder according to DSM-IV-TR (for OUD group)
Not Eligible

You will not qualify if you...

  • Current neuro-psychiatric illness or severe systemic disease, except for the specified study groups' conditions
  • Presence of ferromagnetic metal in the body or a heart pacemaker
  • Previous exposure to ionizing radiation that would exceed safe cumulative limits with study tracer
  • Claustrophobia preventing PET scanning

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Within 4 weeks of screening

Participants undergo PET imaging with the radiotracer [11-C]OMAR to characterize cannabinoid CB1 receptors.

1 visit (in-person)

Long-term Monitoring

Duration - Up to study completion

Participants are observed following imaging to monitor outcomes related to psychiatric and substance use conditions.

Additional assessments may occur depending on cohort assignment

Trial Site Locations

Total: 1 location

1

Connecticut Mental Health Center, Clinical Neuroscience Research Unit

New Haven, Connecticut, United States, 06519

Actively Recruiting

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Research Team

A

Alex Selloni, BA

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

7

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