EUCTR2009-016713-20-SE进行中（未招募）不适用
Efficacy of agomelatine 25 mg/day (with possible increase to 50 mg/day after 8 weeks of treatment) given orally during 16 weeks in patients with Obsessive-Compulsive Disorder.A randomised, double-blind, placebo-controlled, parallel groups, international study.
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- out patients, male or female, aged between 18 (or legal age for majority in the country) and 65 years inclusive
- •- primary diagnosis of Obsessive Compulsive Disorder according to DSM-IV-TR
- •- Y-BOCS total score = 20
- •- requiring a treatment.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 80
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- women of childbearing potential without effective contraception as well as pregnant or breathfeeding women
- •- exclusive hoarders
- •- early onset OCD: diagnosed by a psychiatrist and treated before the age of 12
- •- severe or uncontrolled organic diseases, likely to interfere with the conduct of the study
- •- mental retardation or any pervasive developmental disorder
- •- hepatic impairment
- •- current diagnosis of neurological disorders
研究者
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