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FLUOXETINE VS PLACEBO IN DEPERSONALIZATION DISORDER

FLUOXETINE VS PLACEBO IN DEPERSONALIZATION DISORDER
氟西汀与安慰剂在人格解体障碍中的比较
批准号:
2890783
负责人:
DAPHNE SIMEON
金额:
$12.32万
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-04-01 至 2001-03-31

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中文摘要
翻译
人格解体障碍(DPD)是一种慢性的、潜在的致残性疾病
英文摘要
Depersonalization disorder (DPD) is a chronic, potentially disabling and very understudied psychiatric disorder, generally believed to be rare and treatment-refractory. Patients with DPD suffer from a persistent or recurrent sense of unreality and detachment from various aspects of the self, which leads to great distress or interference with interpersonal or occupational functioning. Although there is a marked paucity of systematic research on the epidemiology, phenomenology and treatment of DPD, preliminary data suggest that serotonin reuptake inhibitors may be of significant therapeutic benefit. However, no randomized, controlled, double-blind pharmacological treatment studies have been conducted to date in DPD. Fluoxetine, a selective serotonin reuptake inhibitor, appears to have efficacy in the treatment of DPD in preliminary studies. Open treatment data from the literature and from our own pilot work suggest a 56% to 71% response rate. Our double-blind pilot treatment data with the serotonin reuptake inhibitor clomipramine appear similarly promising, with a 50% response rate for adequate clomipramine trials, but also suggest a marked intolerance for the side-effects of tricyclics. To systematically assess the efficacy of fluoxetine in the treatment of DPD, 80 patients will be entered into an outpatient double-blind randomized 12-week parallel fluoxetine versus placebo treatment study. Outcome will be rated weekly by the treating psychiatrist and every two weeks by an independent evaluator blind to dosage and side-effects. Responders will continue in a double-blind maintenance phase for an additional 6 months to assess durability of response. When completed, the study should provide systematic information on the efficacy of fluoxetine in the acute treatment of DPD, on the durability of response with six months of continued maintenance, on the change in psychiatric disability with successful treatment, and on the effect of comorbid Axis 1 and Axis Il diagnoses on treatment outcome.
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INTRANASAL OXYTOCIN TREATMENT OF BORDERLINE PERSONALITY DISORDER
EFFICACY OF ZIPRASIDONE VS PLACEBO IN BORDERLINE PERSONALITY DISORDER
EFFICACY OF ZIPRASIDONE VS PLACEBO IN BORDERLINE PERSONALITY DISORDER
PILOT STUDY OF MARIJUANA INDUCED DEPERSONALIZATION DISORDER
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