EUCTR2012-004982-41-EE进行中（未招募）不适用
Interventional, randomised, double-blind, parallel-group,placebo-controlled, flexible-dose study of brexpiprazole asadjunctive treatment to paroxetine or sertraline in adultpatients suffering from post-traumatic stress disorder(PTSD)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 790
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
- •The patient has PTSD, diagnosed according to DSM-IV-TR™ and confirmed by the Mini International Neuropsychiatric Interview (MINI).
- •The patient has a pre-defined Clinician-Administered PTSD Scale Part 2 (CAPS-2) total score at Screening and Baseline Visits.
- •The reported duration of the PTSD is at least 3 months.
- •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 790
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •The index traumatic event that led to development of PTSD took place more than15 years before screening.
- •The patient has a severe personality disorder that in the investigator's opinion may
- •interfere with the conduct of the study.
- •The patient is at significant suicidal risk.
研究者
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