Eating Disorders Trial, Recruiting NCT06566612 Sponsor: University of California, San Diego Condition: Eating Disorders
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Eating Disorders Trial, Recruiting

NCT06566612
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

For people with an eating disorder:

  • You are between 18 and 39 years old
  • You have been diagnosed with anorexia nervosa or bulimia nervosa according to standard medical criteria

For healthy volunteers (people without an eating disorder):

  • You are between 18 and 39 years old
  • Your body weight has stayed within a normal healthy range since your first period

Who may not be able to join:

  • You have a psychotic illness or another mental health condition that has required a hospital stay
  • You are currently dependent on drugs or alcohol, or test positive for drug use on the day of the scan (note: marijuana is an exception to the positive test rule, but may still affect results — confirm with trial site)
  • You have a physical health condition, such as diabetes or pregnancy, that is known to affect eating or body weight
  • You have a neurological condition, a neurodevelopmental condition, or have had a head injury that caused you to lose consciousness for more than 30 minutes
  • You have any reason why you cannot safely have an MRI scan (for example, certain metal implants)
  • You have been diagnosed with obsessive compulsive disorder or major depression as your primary condition
  • (For eating disorder participants only) You are taking psychiatric medication and your dose has changed in the 2 weeks before the scan
  • (For healthy volunteers only) You currently meet the criteria for any psychiatric disorder
  • (For healthy volunteers only) You have any history of binge eating, purging, self-induced vomiting, or misuse of laxatives or diuretics
  • (For healthy volunteers only) You have used any medication known to affect mood or concentration in the last 3 months

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 858-534-8047

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 August 2024
Est. completion
31 July 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Learning rate; fMRI brain response; Brain connectivity

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov