Trials Sponsors Conditions Drugs Pricing

Conditions

Eating Disorders

Keywords

anorexia nervosabulimia nervosa

Study Arms (3)

1

Women who are healthy controls

Procedure: Functional magnetic resonance imaging (fMRI) scan

2

Women who have recovered from bulimia

Procedure: Functional magnetic resonance imaging (fMRI) scan

3

Women who have recovered from anorexia

Procedure: Functional magnetic resonance imaging (fMRI) scan

Interventions

Functional magnetic resonance imaging (fMRI) scanProcedure

Healthy control women, recovered bulimia women, and also recovered anorexia women will complete specific tasks in an fMRI scanner that will take up to 60 minutes.

Also known as: Neurobiology of Eating Disorders, fMRI imaging of Anorexia and Bulimia Nervosa

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Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years - 45 Years

Sexfemale

Healthy VolunteersYes

Age GroupsAdult (18-64)

Sampling MethodNon-Probability Sample

Study Population

The study will include women between the ages of 18 and 45 who have recovered from anorexia or bulimia nervosa for over 1 year and have no current medical problems.

You may qualify if:

Right-handed

Sponsors & Collaborators

National Institute of Mental Health (NIMH)
NIHcollaborator
University of California, San Diego
Otherlead

Study Sites (1)

UCSD Eating Disorders Treatment and Research Center

La Jolla, California, 92037, United States

Biospecimen

Retention: SAMPLES WITH DNA

If desired subjects have a chance to be a part of a DNA blood draw aspect of the study

MeSH Terms

Conditions

Feeding and Eating DisordersAnorexia NervosaBulimia Nervosa

Condition Hierarchy (Ancestors)

Signs and Symptoms, DigestiveSigns and SymptomsPathological Conditions, Signs and SymptomsMental Disorders

Study Officials

Watler Kaye, MD
University of California, San Diego
PRINCIPAL INVESTIGATOR

Enrollment

60 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE CONTROL
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER

Study Record Dates

First Submitted

August 14, 2007

First Posted

August 16, 2007

Study Start

May 2005

Date type not reported

This date has not been verified as actual or estimated.

Evaluating the Brain's Response to Natural Versus Artificial Sweetener in Women Who Have Had an Eating Disorder

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Study Arms (3)

1

2

3

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Biospecimen

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Study Arms (3)

1

2

3

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Biospecimen

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations