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Effect of Intranasal Oxytocin on Appetite and Caloric Intake in Men and Women

Effect of Intranasal Oxytocin on Appetite and Caloric Intake in Humans

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01513499
Enrollment
25
Registered
2012-01-20
Start date
2012-01-31
Completion date
2014-01-31
Last updated
2019-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eating Behavior

Keywords

Eating behavior, Appetite, Oxytocin, Neuropeptide

Brief summary

Exciting advances have led to the concept that hormones can modulate appetite and food intake. Oxytocin is a peptide hormone that is released in regions throughout the brain, including areas involved in food motivation. Animal studies suggest that oxytocin may reduce food intake. The effects of oxytocin administration on eating behavior in humans, which could have important implications in eating-related disorders ranging from obesity to anorexia nervosa, have not been investigated. This double-blind placebo-controlled cross-over study of single-dose oxytocin administration investigates whether: 1. Caloric intake will decrease following administration of oxytocin versus placebo 2. Appetite will decrease following administration of oxytocin versus placebo 3. Resting energy expenditure will increase following administration of oxytocin versus placebo

Interventions

DRUGOxytocin

Intranasal oxytocin 24 IU single-dose administration

DRUGPlacebo

Intranasal Placebo single-dose administration

Sponsors

Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-45 years old * BMI 18.5-24.9, 25-40 * Regular breakfast eater (at least 4 times per week) * Stable weight within the past three months

Exclusion criteria

* Psychiatric disease * Use of psychotropic medications * History of eating disorder * History of excessive exercise within the last three months * History of diabetes mellitus * Active substance abuse * Hematocrit below normal range * Gastrointestinal tract surgery (including gastrectomy, gastric bypass surgery, and small or large bowel resection) * History of cardiovascular disease (such as hypertrophic cardiomyopathy, valvular heart disease, coronary heart disease, or coronary artery spasms) * Untreated thyroid disease * Tobacco use

Design outcomes

Primary

MeasureTime frame
Caloric intake+60 minutes after drug/placebo

Secondary

MeasureTime frameDescription
Appetite+55 (fasting) and +90 minutes (post-prandial) after drug/placeboAssessed using a Visual Analogue Scale
Resting energy expenditure+30 minutes after drug/placeboAssessed using metabolic cart

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026