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Schematic overview of the trial design
Either cannabidiol (CBD) or placebo (PLC) was administered after a preparatory phase at the beginning of the test session, followed by a rest period. 170 min after medication administration, venous blood was drawn for determination of CBD levels, and a combined stress- and cue exposure was conducted from minute 220–240 (i.e., 180 min after medication administration) using a combination of the Trier Social Stress Test (41) and an alcohol cue exposure in a bar lab setting (for details see text). Directly afterward, an alcohol cue-reactivity functional magnetic resonance imaging task was performed to investigate cue-induced brain activation and craving.

Schematic overview of the trial design Either cannabidiol (CBD) or placebo (PLC) was administered after a preparatory phase at the beginning of the test session, followed by a rest period. 170 min after medication administration, venous blood was drawn for determination of CBD levels, and a combined stress- and cue exposure was conducted from minute 220–240 (i.e., 180 min after medication administration) using a combination of the Trier Social Stress Test (41) and an alcohol cue exposure in a bar lab setting (for details see text). Directly afterward, an alcohol cue-reactivity functional magnetic resonance imaging task was performed to investigate cue-induced brain activation and craving.

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Although alcohol use disorder (AUD) is highly prevalent, only a few medications are approved for its treatment leaving much room for improvement. Cannabidiol (CBD) might be a particularly promising candidate, with preclinical data suggesting that CBD is effective in targeting AUD symptoms and disease processes that drive alcohol use and relapse, du...

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