Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
INTERVENTIONAL
2003-07-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
TREATMENT
Interventions
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topiramate
Eligibility Criteria
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Inclusion Criteria
* Met the criteria of bulimia nervosa or eating disorder NOS with binge-eating behavior in DSM-IV-TR,
* Had weight \> or = 100th % of expected body weight for their age,
* Engaged in binge eating at least once a week for 9 out of the 12 weeks prior to the study entry, and
* Were judged by a clinician to be stable enough to be treated for their psychiatric condition as an outpatient (i.e, no acute suicidality, hallucination, unstable vital signs or persistently abnormal laboratory results due to eating disorder).
Exclusion Criteria
* Subjects were also excluded if they were taking carbonic anhydrase inhibitors, carbamazepine, phenytoin, phenobarbital, valproic acid, evening primrose oil or oral contraceptives.
12 Years
23 Years
ALL
No
Sponsors
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The Zucker Hillside Hospital
OTHER
Responsible Party
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The Zucker Hillside Hospital
Locations
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The Zucker Hillside Hospital
Glen Oaks, New York, United States
Countries
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Other Identifiers
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03-04-063
Identifier Type: -
Identifier Source: org_study_id