Register to:

  • Save your health matches
  • Ask questions
  • Connect with others
  • Get the latest on clinical trials
Register Now

Already a member?
Sign In

Inspire others by sharing your story

Share Story

Share with others things you have tried, so they can learn from your experiences

Write Review

Clinical Trials

| All Clinical Trials | Go Back To Home Page

Study ID: NCT00307190

Title: Postprandial Cholecystokinin Release and Gastric Emptying in Binge Eating Disorder

Status:
Recruiting
Phase:
0

Trial Contact Information

Principal Contact:
Eating Disorders Clinic
Principal Phone:
212-543-5739
Principal Email:
edru@pi.cpmc.columbia.edu

Sponsor(s): National Institute of Mental Health (NIMH)

Condition(s):
Eating Disorders
Bulimia nervosa
Binge-eating disorder
Bulimia
Eating Disorder
Obesity
Binge Eating Disorder

Purpose: This study will determine whether the disturbances in cholecystokinin release and gastric emptying that occur in people with binge eating disorder are similar to those that occur in people with bulimia nervosa.

Eligibility:
Minimum Age:
18 Years
Maximum Age:
60 Years
Accepts Healthy Volunteers:
Yes

Inclusion Criteria:

For all participants:

- Obese (body mass index (BMI) greater than 35 kg/m2)

For participants with BED:

- Meets DSM-IV criteria for BED

- BED duration of at least 1 year

For healthy participants:

- Weight close to that of participants with BED

Exclusion Criteria for all participants:

- Current or past diagnosis of BN, or any binge eating or self-induced vomiting

- Significant medical illness

- Current or lifetime history of schizophrenia, bipolar disorder, or other psychotic
disorder as defined by DSM-IV-TR

- Current DSM-IV-TR diagnosis of organic mental disorder, factitious disorder, or
malingering

- History of a personality disorder (e.g., schizotypal, borderline, or antisocial) that
might interfere with assessment or compliance with the study procedures

- At risk for suicide

- Currently taking psychotropic medication or medication that is known to affect
appetite or gastric functioning

- History of drug or alcohol abuse within the 3 months prior to study entry

- Pregnant, planning to become pregnant, or lactating

- Anemia

Other Location(s): New York, New York United States

Terms: This is an abstract courtesy of ClinicalTrials.gov, a service of the US National Institute of Health Developed by the National Library of Medicine. ClinicalTrials.gov provides regularly updates information about federally and privately supported clinical research in human volunteers.

arrow 26 People Experienced Clinical Trials

See All

Feedback