NCT00302770终止3 期
Efficacy of Quetiapine in Generalised Social Anxiety Disorder, a Double-blind, Placebo-controlled Study
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 发起方
- AstraZeneca
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Change on Lebowitz Social Anxiety Scale (LSAS) from baseline to endpoint
研究概览
简要总结
This trial will explore the efficacy of quetiapine in Social Anxiety Disorder, generalized type. The following elements of response will be tested: number of responders to treatment, time to response, effect size as measured with the LSAS
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Written Confirmed Consent,
- •All patients meet the DSM IV criteria for generalized social anxiety disorder,
- •A score ≥ 60 on the LSAS,
- •male and female aged between 18 and 65 years
排除标准
- •Presence of any primary axis I diagnosis other than social anxiety disorder according to DSM-IV,
- •alcohol and/or substance abuse according to DSM-IV criteria within the last 12 months,
- •any personality disorder as the primary diagnosis, with the exception of avoidant personality disorder,
- •patients at risk of suicide
结局指标
主要结局
Change on Lebowitz Social Anxiety Scale (LSAS) from baseline to endpoint
次要结局
- Number of responders, time to onset of response of sustained response to treatment
研究者
研究点 (1)
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