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Trials / Terminated

TerminatedNCT04404712

FAAH Availability in Psychiatric Disorders: A PET Study

Status
Terminated
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
6 (actual)
Sponsor
Yale University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The aim of the present study is to examine Fatty Acid Amide Hydrolase (FAAH) availability in humans, including healthy individuals and across a spectrum of psychiatric disorders in which alterations in the endocannabinoid system are observed.

Detailed description

This study involves in vivo examination of FAAH availability, implicated both in the pathophysiology and therapeutics of disorders including PTSD, substance use disorders (e.g., alcohol use disorder, cannabis/cannabinoid use disorder, nicotine use disorder), psychotic disorders including schizophrenia, and mood disorders. The endocannabinoid system is a neuromodulatory system that has been implicated across a wide range of psychiatric disorders and may be implicated in the regulation of mood, appetitive behaviors, sleep, and cognition. Thus, alterations in the ECS have wide ranging implications. Finally, the ECS is being explored as a novel therapeutic target for several psychiatric disorders. Additionally, the test/retest reliability of the radiotracer, \[11C\]MK-3168, will be studied in up to 10 healthy control individuals.

Conditions

Interventions

TypeNameDescription
DRUG[11C]MK-3168One PET scan involving administration of PET ligand \[11C\]MK-3168

Timeline

Start date
2020-09-23
Primary completion
2021-06-30
Completion
2021-06-30
First posted
2020-05-27
Last updated
2023-02-21

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04404712. Inclusion in this directory is not an endorsement.

FAAH Availability in Psychiatric Disorders: A PET Study (NCT04404712) · Clinical Trials Directory