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To evaluate the efficacy and safety of fluoxetine in treating children and adolescents who have non-psychotic major depressive disorder (MDD).
Randomised, double blind, placebo controlled trial with 8 weeks of follow up.
Outpatient mood disorders programme in Dallas, USA.
96 patients (mean age 12 y, 54% boys) who met the Diagnostic and Statistical Manual of Mental Disorders, 3rd edition, revised criteria for MDD. Exclusion criteria were bipolar disorder; psychotic depression; independent sleep wake disorder; substance abuse; anorexia nervosa; bulimia; previous treatment with fluoxetine, 20 mg/day, for ≥3 weeks; or a first degree relative with bipolar I disorder.
48 patients received fluoxetine, 20 mg/day, and 48 patients received a …
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