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CB1R in Synthetic Psychoactive Cannabinoids (CB1R in Spice)

Yale University logo

Yale University

Status

Active, not recruiting

Conditions

Drug Dependence

Treatments

Other: [11-C]OMAR

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03539575
1R21DA041580-01A1 (U.S. NIH Grant/Contract)
1308012514A

Details and patient eligibility

About

The purpose of this research study is to determine whether the CB1R availability is lower in synthetic psychoactive cannabinoid subjects using the most widely available synthetic psychoactive cannabinoids at the time the study is initiated.

Enrollment

15 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

  • Able to provide written consent
  • Age 18-55
  • Current Synthetic Psychoactive Cannabinoids consumption

Exclusion:

  • MRI metal exclusions and claustrophobia
  • Education completed is less than 12 years

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Synthetic Psychoactive Cannabinoid Users
Other group
Description:
Synthetic Psychoactive Cannabinoid dependent subjects who are frequent spice/K2 users will receive the radiotracer \[11-C\]OMAR.
Treatment:
Other: [11-C]OMAR

Trial contacts and locations

1

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Central trial contact

Patrick Skosnik, Ph.D.; Deepak C D'Souza, M.D.

Data sourced from clinicaltrials.gov

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