Condition: Binge-eating Disorder · Sponsor: Massachusetts General Hospital
This study evaluates the impact of intranasal oxytocin vs placebo in patients with binge eating disorder or episodes of binging. We hypothesize that 8 weeks of intranasal oxytocin vs placebo will improve clinical outcomes \[reduction in bingeing frequency\], and have a satisfactory safety and tolerability profile. We will also explore the predictive value of changes in homeostatic appetite, reward sensitivity, and impulse control, the identified underlying mediators, as assessed 4 weeks into the intervention, for treatment success after 8 weeks of the intervention.
This description comes directly from the study's public registry record.
Lauren Shabazian, NP · 617-726-0047 · lshabazian@mgh.harvard.edu
Jordan Hillard · 617-726-0047 · jhillard1@mgh.harvard.edu
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| Neuroendocrine Unit Research Center | Boston, Massachusetts, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05664516