20
Participants
Start Date
November 1, 2022
Primary Completion Date
November 30, 2024
Study Completion Date
November 30, 2025
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."
RECRUITING
Unit of Psychiatry, University Hospital of Udine, Udine
RECRUITING
Unit of Psychiatry, University Hospital of Udine, Udine
National Research Council (CNR), Institute of Biomolecular Chemistry (ICB), Italy
UNKNOWN
University of Udine
OTHER