4.1 Article

A randomized, double-blind, placebo-controlled clinical trial of 8-week intranasal oxytocin administration in adults with obesity: Rationale, study design, and methods

期刊

CONTEMPORARY CLINICAL TRIALS
卷 122, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cct.2022.106909

关键词

Obesity; Oxytocin; Weight loss; Appetite regulation; Energy metabolism; Neuroimaging

资金

  1. National Institutes of Health (NIH) [R01 DK109932, K24 MH120568]
  2. Nutrition Obesity Research Center at Harvard [P30 DK040561]
  3. Boston Nutrition Obesity Research Center pilot grant [P30 DK046200]
  4. Massachusetts General Hospital Department of Medicine Eleanor and Miles Shore Fellowship Award

向作者/读者索取更多资源

This article presents the theoretical basis, design, methods, and analysis plan of a randomized clinical trial on intranasal oxytocin for weight loss in adults with obesity. The study aims to investigate the efficacy, safety, and mechanisms of oxytocin administration, as well as explore changes in other relevant indicators. The study sample includes 61 male and female participants aged 18-45 years.
Background: Obesity affects more than one-third of adults in the U.S., and effective treatment options are urgently needed. Oxytocin administration induces weight loss in animal models of obesity via effects on caloric intake, energy expenditure, and fat metabolism. We study intranasal oxytocin, an investigational drug shown to reduce caloric intake in humans, as a potential novel treatment for obesity. Methods: We report the rationale, design, methods, and biostatistical analysis plan of a randomized, double-blind, placebo-controlled clinical trial of intranasal oxytocin for weight loss (primary endpoint) in adults with obesity. Participants (aged 18-45 years) were randomly allocated (1:1) to oxytocin (four times daily over eight weeks) versus placebo. Randomization was stratified by biological sex and BMI (30 to <35, 35 to <40, >= 40 kg/m2). We investigate the efficacy, safety, and mechanisms of oxytocin administration in reducing body weight. Secondary endpoints include changes in resting energy expenditure, body composition, caloric intake, metabolic profile, and brain activation via functional magnetic resonance imaging in response to food images and during an im-pulse control task. Safety and tolerability (e.g., review of adverse events, vital signs, electrocardiogram, comprehensive metabolic panel) are assessed throughout the study and six weeks after treatment completion.Results: Sixty-one male and female participants aged 18-45 years were randomized (mean age 34 years, mean BMI 37 kg/m2). The study sample is diverse with 38% identifying as non-White and 20% Hispanic.Conclusion: Investigating intranasal oxytocin's efficacy, safety, and mechanisms as an anti-obesity medication will advance the search for optimal treatment strategies for obesity and its associated severe sequelae.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.1
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据