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Intranasal Oxytocin for Alcohol Use Disorder: A Randomized, Double-Blind, Placebo-Controlled Multisite Trial
Nassima Ait-Daoud Tiouririne1, Jospeh A Legan1, Eric Devine2
1Center for Leading Edge Addiction Research, University of Virginia, Charlottesville, Virginia, USA.
Intranasal oxytocin did not significantly reduce alcohol use disorder (AUD) symptoms in a 12-week trial. While well-tolerated, further research with higher doses or longer durations may be needed to confirm its efficacy.
Area of Science:
- Neuroscience
- Pharmacology
- Clinical Psychology
Background:
- Oxytocin, a neuropeptide, influences behaviors related to addiction, including reward and stress response.
- Previous animal studies suggest oxytocin reduces alcohol consumption, but human trial results for alcohol use disorder (AUD) have been inconsistent.
- This study aimed to assess the efficacy and safety of intranasal oxytocin for treating AUD.
Purpose of the Study:
- To evaluate the efficacy of intranasal oxytocin in reducing heavy drinking days in individuals with AUD over a 12-week period.
- To assess secondary drinking outcomes, psychological measures, and alcohol-related consequences.
- To determine the safety and tolerability of intranasal oxytocin in the AUD population.
Main Methods:
- A 12-week, double-blind, randomized, multisite clinical trial involving 100 individuals diagnosed with AUD.
- Participants received either intranasal oxytocin (up to 70 IU/day) or a placebo.
- The primary outcome was the weekly percentage of heavy drinking days (PHDD) over 10 weeks of maintenance treatment.
Main Results:
- No significant difference in PHDD was observed between the oxytocin and placebo groups during the 10-week maintenance phase.
- A slight, non-significant reduction in drinking was noted in the oxytocin group from weeks 9 to 12.
- Oxytocin was well-tolerated, with mild adverse events comparable between groups; participants receiving oxytocin showed reduced anger and physical aggression.
Conclusions:
- Intranasal oxytocin was found to be safe and well-tolerated for AUD treatment but did not significantly reduce drinking or related outcomes.
- The study suggests that higher doses, longer treatment durations, or larger trials may be necessary to identify potential therapeutic effects or responsive subgroups.
- Further investigation is warranted to fully determine the potential role of oxytocin in managing alcohol use disorder.
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