Sponsor(s):
National Institute of Mental Health (NIMH)
- Condition(s):
-
Eating Disorders
Bulimia nervosa
Binge-eating disorder
Bulimia
Eating Disorder
Binge Eating Disorder
Purpose:
This study will determine the effectiveness of the antibiotic erythromycin in enhancing
gastrointestinal function and decreasing the frequency of binge eating in people with
bulimia nervosa.
- Eligibility:
-
- Minimum Age:
- 18 Years
- Maximum Age:
- 55 Years
- Accepts Healthy Volunteers:
- Yes
Inclusion Criteria:
- Meets DSM-IV criteria for bulimia nervosa
- Duration of illness is greater than 1 year
- Self-induces vomiting
- Weighs 80%-120 % of ideal weight
Exclusion Criteria:
- Significant medical illness
- Current or lifetime history of schizophrenia, bipolar disorder, or other psychotic
disorder, as defined by DSM-IV-TR criteria
- Moderate to severe depression, as defined by a score greater than 18 on the Hamilton
Depression Scales
- 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
- Current psychotropic medications and current medications that affect GI function or
that inhibit or induce CYP3A gene expression
- Currently pregnant, lactating, or planning to become pregnant
- Drug or alcohol abuse within the 3 months prior to study entry
- Abnormal EKG at baseline or 1 week following each upward dosage adjustment
- Anemia
- Known intolerance to erythromycin, or related antibiotics
- Abnormal results on liver function tests
- Electrolyte abnormalities
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.