EUCTR2006-004605-26-GB进行中(未招募)1 期
Proposal to investigate the efficacy and tolerability of Aripiprazole as an add-on therapy in patients not responding to an adequate dose of an antidepressant therapy
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 90
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
- •-Meets criteria for Major depressive disorder by DSM IV
- •-Currently on an adequate dose (within BNF limits) of an antidepressant for at least 6 weeks with and/or other augmentation therapy including lithium and carbamezepine but not antipsychotic medication
- •-Have Hamilton Depression rating Scale (HAMD17) total score of >15
- •- Agrees to use an effective form of contraception throughout the study
- •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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- DSM IV defined history of substance abuse or dependence within the past year
- •-Unstable medical illness (e.g., cardiovascular, liver, kidney, respiratory, endocrine, or neurological disease, including uncontrolled seizure disorder)
- •-History of or current psychotic features
- •- Patients should not have been on an antipsychotic medication in the past 2 weeks
- •-Patients who are receiving psychotherapy
研究者
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