Paroxetine but not imipramine improved depression related outcomes in adolescents with DSM-IV major depression.
نویسنده
چکیده
Patients 275 adolescents (mean age 15 y, 62% girls) who were medically healthy with a current episode of DSM-IV major depression for >8 weeks. Additional inclusion criteria were a total score of >12 on the Hamilton Depression Rating Scale (HDRS), a score of < 60 on the Children’s Global Assessment Scale, and a score of >80 on the Peabody Picture Vocabulary Test. Exclusion criteria included a current or lifetime DSM-IV diagnosis of bipolar disorder, schizoaffective disorder, eating disorder, alcohol or substance use disorder, and organic brain disorder. 99% of patients were included in the analysis.
منابع مشابه
Efficacy of paroxetine in the treatment of adolescent major depression: a randomized, controlled trial.
OBJECTIVE To compare paroxetine with placebo and imipramine with placebo for the treatment of adolescent depression. METHOD After a 7- to 14-day screening period, 275 adolescents with major depression began 8 weeks of double-blind paroxetine (20-40 mg), imipramine (gradual upward titration to 200-300 mg), or placebo. The two primary outcome measures were endpoint response (Hamilton Rating Sca...
متن کاملRestoring Study 329: efficacy and harms of paroxetine and imipramine in treatment of major depression in adolescence
OBJECTIVES To reanalyse SmithKline Beecham's Study 329 (published by Keller and colleagues in 2001), the primary objective of which was to compare the efficacy and safety of paroxetine and imipramine with placebo in the treatment of adolescents with unipolar major depression. The reanalysis under the restoring invisible and abandoned trials (RIAT) initiative was done to see whether access to an...
متن کاملA double-blind, placebo-controlled study of quetiapine and paroxetine as monotherapy in adults with bipolar depression (EMBOLDEN II).
OBJECTIVE The aim of this study was to evaluate the efficacy and tolerability of quetiapine and paroxetine monotherapy for major depression in bipolar disorder. METHOD 740 patients (478 bipolar I, 262 bipolar II) with major depressive episodes (DSM-IV) were randomly assigned to quetiapine 300 mg/d (n = 245), quetiapine 600 mg/d (n = 247), paroxetine 20 mg/d (n = 122), or placebo (n = 126) for...
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M e t h o d s Design: Randomized, 2 × 2 factorial design, placebo-controlled trial. Allocation: {Concealed}†.* Blinding: Blinded (clinicians, patients, and outcome assessors).* Clinicians and patients were not blinded to the psychotherapy intervention. Follow-up period: 2 years. Setting: Specialized university-based clinic in Pittsburgh, Pennsylvania, USA. Patients: 116 patients ≥ 70 years of a...
متن کاملRecent placebo-controlled acute trials in bipolar depression: focus on methodology.
The completion of three recent large-scale, double-blind controlled acute trials in bipolar I depression has improved our understanding of the management of major depressive episodes associated with bipolar disorder. In contrast to the cross-over designs used in the early studies of lithium in bipolar depression, the designs utilized in these recent studies have employed random assignment to pa...
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ورودعنوان ژورنال:
- Evidence-based mental health
دوره 5 1 شماره
صفحات -
تاریخ انتشار 2002