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NCT Number: NCT04551482

Oxytocin for Weight Loss in Adolescents

This is a randomized, double blind, placebo-controlled study of the effects of intranasal oxytocin in youths with obesity, ages 10-18 years old. Subjects will be randomized to receive intranasal oxytocin or placebo (1 spray per nostril, 4 times per day) for 12 weeks. Study visits include screening to determine eligibility, 2-part main study visits at baseline, week 8, and week 12, and safety check-in visits at weeks 1, and 4; phone calls at weeks 2, 6, and 10, with a safety follow-up visit 6 weeks after the last dose of study drug. Study procedures include appetite, behavioral, metabolic, and endocrine assessments.

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Key information

Age range

10 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

Location status: Recruiting

Location contact

Elizabeth A Lawson, MD

CONTACT

[email protected]

About this study

In recent years there has been a dramatic increase in obesity and its complications in both children and adults. Earlier treatment substantially reduces the likelihood of developing complications later in life while concurrently improving quality of life and decreasing mortality. Therefore, it is essential to develop safe and effective therapeutic strategies for weight loss, particularly in adolescents. Oxytocin (OXT), a hypothalamic peptide hormone that regulates energy balance, is a novel neuroendocrine weight-loss therapeutic in adults with obesity because it simultaneously reduces energy intake and increases energy expenditure and is well-tolerated. Data are currently lacking regarding effects of OXT administration in adolescents with obesity.

The current study is a 12-week randomized controlled trial (RCT) of OXT vs. placebo in 10-18-year old adolescents with obesity. We hypothesize that OXT administration will decrease weight as a consequence of decreased caloric intake and increased energy expenditure, both partially mediated by reduced hypothalamic inflammation (such inflammation drives weight gain by increasing food intake and reducing energy expenditure). Further, OXT will improve metabolic risk markers, such as visceral and intrahepatic fat, systemic inflammation, and serum lipids.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and Females, 10-18 years
  • Obesity (BMI ≥95th percentile for age and gender)
  • Willingness to maintain current diet and lifestyle for the duration of study participation

Exclusion criteria

  • Current substance abuse
  • Use of prescription or over-the-counter drugs or dietary/herbal supplements that may affect weight if dose increased in the three months preceding the baseline visit and/or if they plan to increase the dose during the 18 weeks of study participation.
  • Greater than 5kg weight loss over 3 months;
  • Follows a nonstandard diet (e.g., Paleo, Atkins, raw diet, macrobiotic diet)
  • Cardiovascular disease
  • Prolonged QT interval
  • Chronic inflammatory bowel disease and other inflammatory conditions
  • Epilepsy
  • TSH > 2.5 times upper limit of normal
  • Alanine transaminase (ALT) or aspartate transaminase (AST) >2.5 times upper limit of normal
  • Creatinine >1.5 mg/dl
  • Hyponatremia
  • Pregnancy/breastfeeding or refusal to use contraception not containing estrogen throughout the study if female and sexually active
  • MRI exclusion criteria such as the presence of a pacemaker or cerebral aneurysm clips
  • Weight >450 lbs due to limits for MRI and DXA scanners
  • Type 1 Diabetes Mellitus or Type 2 Diabetes Mellitus if HbA1c >8%
  • Active eating disorder

Treatment and study plan

Oxytocin nasal spray

Drug

24 IU nasal spray, 4 times per day for 12 weeks

Other names: Syntocin

Placebo

Drug

24 IU nasal spray, 4 times per day for 12 weeks

Primary outcomes

  1. Body mass index (BMI)

    Time frame: 12 weeks

    Mean difference in BMI between Oxytocin and Placebo group after 12 weeks of treatment. BMI will be calculated as weight/height2

Secondary outcomes

  1. Lean mass and Fat mass

    Time frame: 12 weeks

    Dual Energy Absorptiometry (DXA) will be used for measuring fat mass (kg) and lean mass (Kg)

  2. Fasting Resting Energy Expenditure (kCal)

    Time frame: 12 weeks

    Assessed by Indirect calorimetry

Study contacts

Contact information is provided by the study sponsor or research team.

Elizabeth A Lawson, MD, MMSc

CONTACT

[email protected]

617-726-3870

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Official study title

Oxytocin as a Neuroendocrine Therapy for Obesity in Youth

Important dates

Study start
2021
Primary completion
2026
Study completion
2027
First posted
Sep 16, 2020
Registry last updated
Jun 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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