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NCT07915986Not yet recruitingPhase 1

Brain Dopamine Dynamics in Obesity

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

This study measures the brain's dopamine response to milkshake consumption in people with a healthy weight and people with obesity and examines whether this response differs between the two groups. Dopamine release will be measured using ultra-high-resolution positron emission tomography (PET) imaging with the NeuroEXPLORER scanner. The study will also examine how the dopamine response relates to hormonal responses measured at the same time and to participants' food intake behavior.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
100 (estimated)
First submitted
15 Oct 2026
Start date
Nov 2026
Primary completion date
Nov 2029
Lead sponsor
Yale University
Diseases
Obesity
NCT number
NCT07915986

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 100
  • From Nov 2026 to the primary completion date, Nov 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current use of systemic hormone therapy, including oral, transdermal, or injectable estrogen or combined estrogen-progestogen preparations
  • Radiation exposure for research purposes within the past year such that participation in this study would place them over guideline limits for annual radiation exposure (an effective dose of 5 rem received per year).
  • Current, past or anticipated exposure to radiation in the workplace within one year
  • Contraindications for MRI: metal implants incompatible with MRI, claustrophobia, large colored tattoos, or body weight \>285 pounds
  • Current or past (within last year prior to enrollment) pharmacological obesity treatment
  • Past surgical obesity treatment (bariatric surgery)
  • Blood donation within 8 weeks prior to study

Other illness

  • History of or current psychiatric disorder
  • History of or current neurological disorder
  • History of bleeding disorder or use of anticoagulants
  • History of or current eating disorder (Eating Disorder Examination Questionnaire)
  • Presence of type 1 or type 2 diabetes mellitus
  • Uncontrolled thyroid disease
  • Presence of any somatic disorder or medication use that interferes with brain functional networks or metabolic response to food
  • Active oral or perioral conditions that may alter taste perception or compromise safety during gustometer use

Lab values

  • Renal insufficiency (eGFR \<15 mL/min/1.73m²)

Age

  • Childhood-onset obesity (onset before age 10 years)

Other

  • Premenopausal status in women
  • Smoking (current use of any tobacco or nicotine products)
  • Elevated liver enzymes (\>2× the upper limit of normal)
  • Anemia and/or Hematocrit \<35 vol%
  • Lactose intolerance
  • Shift work
  • Current use of cannabis (any form), cocaine, amphetamines, or other recreational substances with known dopaminergic effects
  • Heavy alcohol use, defined as \>15 standard drinks per week for men or \>8 standard drinks per week for women (National Institute on Alcohol Abuse and Alcoholism thresholds)
  • Pacemaker in situ or other implanted electronic device
  • Current use of structured meal replacement programs

Who the study is looking for

  • BMI 20-25 kg/m² (normal weight group) or BMI 30-45 kg/m² (obesity group)
  • Stable body weight in the 3 months prior to enrollment (\<5%weight change)
  • Male sex or postmenopausal female (defined as cessation of menstrual periods for ≥12 consecutive months or FSH \>25.8 mIU/mL)
  • Able to read, write, and speak English
  • Capable of giving informed consent

Age in the registry: 50 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Yale School of Medicine
Coordinator of this site? Confirm its status
New HavenUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.