Stopped: Low enrollment numbers, pharmacy not able to acquire sufficient study article component (methylcellulose) due to manufacturer backorder
The objective of this study is to evaluate the effectiveness of oral naltrexone tablets in pediatric and adolescent eating disorders, in particular anorexia nervosa and bulimia nervosa, as compared to placebo. Study participants will be patients in a partial hospitalization program or intensive outpatient program for eating disorder.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
ED-15 Score
Timeframe: Time Frame: Measured at the following timepoints: enrollment
ED-15 Score
Timeframe: Time Frame: Measured at the following timepoints: one week
ED-15 Score
Timeframe: Time Frame: Measured at the following timepoints: three week
ED-15 Score
Timeframe: Time Frame: Measured at the following timepoints: six weeks
ED-15 Score
Timeframe: Time Frame: Measured at the following timepoints: nine weeks (last week of treatment)
ED-15 Score
Timeframe: Time Frame: Measured at the following timepoints: 6 months after enrollment