Endocannabinoid Activity Remodulation for Psychosis Liability in Youth

NARecruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

November 1, 2022

Primary Completion Date

November 30, 2024

Study Completion Date

November 30, 2025

Conditions
Clinical High Risk for PsychosisUltra High Risk for PsychosisAttenuated Psychotic Symptoms
Interventions
DIETARY_SUPPLEMENT

Ultra-micronized Palmitoylethanolamide (PEA)

"Palmitoylethanolamide (PEA) is an N-acylethanolamine (AE), produced on demand by different cell types as a response to actual or potential damage, proven to down-regulate central and peripheral activity of mast cells and non-neuronal cells (e.g., astrocytes, microglia) and to exert protective functions against glutamate neuro-toxicity, accounting for its naturally-occurring anti-inflammatory, analgesic, and anticonvulsant properties. Due to the shared pharmacodynamic properties, PEA is considered as the endogenous equivalent of Cannabidiol (CBD). A growing body of literature has confirmed the role of PEA in most neurobiological mechanisms underpinning several neuropsychiatric conditions both in clinical and preclinical settings. The effect of PEA over neuroinflammation and glutamate signaling may represent a promising biobehavioral mechanism underlying the clinical utility of its oral supplementation in CHR state."

Trial Locations (2)

33100

RECRUITING

Unit of Psychiatry, University Hospital of Udine, Udine

RECRUITING

Unit of Psychiatry, University Hospital of Udine, Udine

All Listed Sponsors
collaborator

National Research Council (CNR), Institute of Biomolecular Chemistry (ICB), Italy

UNKNOWN

lead

University of Udine

OTHER