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Imaging the Dopamine Systems in Bulimia Nervosa

Imaging the Dopamine Systems in Bulimia Nervosa

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01493362
Enrollment
33
Registered
2011-12-16
Start date
2008-01-31
Completion date
2013-12-31
Last updated
2014-08-15

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

Conditions

Eating Disorders

Keywords

Bulimia Nervosa, PET Imaging, Dopamine

Brief summary

This study will use positron emission tomography imaging to investigate the dopamine systems in people with bulimia nervosa.

Interventions

None listed

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
New York State Psychiatric Institute
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

Participants with BN: * Meets DSM-IV criteria for BN * Sufficiently medically and psychiatrically stable to participate in research Health Control Participants: * No current or past psychiatric illness * Between 80% and 120% of ideal body weight

Exclusion criteria

All participants: * Current use of psychotropic medication such as anti psychotics or antidepressants * Pregnant or breastfeeding * history of substance abuse * Significant medical illness * High blood pressure (resting systolic blood pressure greater than 150mmHg and diastolic blood pressure greater that 90 mmHg) * Current or lifetime history of schizophrenia, bipolar disorder, or other psychotic disorder as defined by DSM-IV * Metal implants or paramagnetic objects contained within the body that may interfere with the MRI scan, as determined in consultation with a neuroradiologist and according to specified reference book guidelines * Exposed to radiation in the workplace or has had a nuclear medicine procedure during the 1 year before study entry * Previous adverse reaction to psycho stimulants

Design outcomes

Primary

MeasureTime frame
D2 receptor densityMeasured at baseline
DA release in the striatumMeasures after Mythlyphenidate challenge

Countries

United States

Outcome results

None listed

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