Obesity Clinical Trial
Official title:
Effect of a Single Dose of Intranasal Oxytocin on Food Intake in Obese Adolescents
The purpose of the study is to determine the effect of intranasal OXT caloric intake and
eating behaviors in otherwise healthy obese adolescents.
The primary objective of this study is to determine the effects of intranasal administration
of oxytocin on food intake in obese, pubertal or post-pubertal adolescents (13 to <18 years
in girls, and 15 to <20 years in boys).
Participants will undergo a telephone screening and then, within 4 weeks, complete an in-person screening visit to determine eligibility. Then, within 4 weeks they will be randomized to either OXT or placebo. After a minimum 1-week (7-28 days) "washout," participants will cross-over to treatment with the other condition (i.e., placebo or OXT). ;
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