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RECRUITING

Eating Disorders Genetics Initiative 2

NCT06594913 · View on ClinicalTrials.gov ↗

Study Summary

The overarching intention of the Eating Disorder Genetics Initiative 2 (EDGI2) is to increase sample size, diversity, and eating disorder phenotypes. The investigators are enrolling 20,000 new participants with anorexia nervosa (AN), bulimia nervosa (BN), binge-eating disorder (BED), avoidant/restrictive food intake disorder (ARFID), and controls in the US, Mexico, Australia, New Zealand, Sweden, and Denmark. A primary study goal is to enroll at least 30% of participants from underrepresented groups. Participants are asked to complete a series of questionnaires and submit a saliva sample for genotyping. The goal is to better understand eating disorders and how they relate to each other so that better treatments can be developed.

Interventions

  • OTHER Eating disorder diagnosis group

Study Locations (5)

Other

  • Comenzar de Nuevo — Monterrey
  • Karolinska Institutet — Stockholm

North Carolina

  • University of North Carolina at Chapel Hill — Chapel Hill

Queensland

  • QIMR Berghofer — Brisbane

Canterbury

  • University of Otago — Christchurch

Trial Details

FieldValue
Enrollment Target 20,000 participants
Start Date 2024-10-28
Est. Completion 2027-08-01

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06594913

The ClinicalTrials.gov registry entry for NCT06594913 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 20,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of North Carolina, Chapel Hill, which has 725 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Anorexia Nervosa appearing as the primary indexed condition, and to 1 intervention — of which Eating disorder diagnosis group is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06594913 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Other, North Carolina, Queensland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06594913 about?

NCT06594913 is a clinical study titled "Eating Disorders Genetics Initiative 2". The overarching intention of the Eating Disorder Genetics Initiative 2 (EDGI2) is to increase sample size, diversity, and eating disorder phenotypes. The investigators are enrolling 20,000 new participants with anorexia nervosa (AN), bulimia nervosa (BN), binge-eating disorder (BED), avoidant/restri...

What is the current status of trial NCT06594913?

This trial is currently recruiting. The enrollment target is 20,000 participants. The study started on 2024-10-28. Estimated completion is 2027-08-01.

What conditions does trial NCT06594913 study?

This clinical trial studies the following conditions: Anorexia Nervosa, Bulimia Nervosa, Binge-Eating Disorder, Avoidant Restrictive Food Intake Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06594913?

The interventions under investigation include: Eating disorder diagnosis group (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06594913?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 725 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06594913 being conducted?

This trial has 5 study locations across North Carolina, Queensland, Canterbury. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial