NCT00758251已完成不适用
Observation of Change in Clinical Global Impression Scores in Schizophrenia Patients Receiving Seroquel XR Treatment
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AstraZeneca
- 入组人数
- 80
- 试验地点
- 2
- 主要终点
- Improvement in CGI scores and BPRS comparing visits 1 and 3.
研究概览
简要总结
The purpose of this study is to assess severity of illness in schizophrenia patients in routine clinical practice at the time of entry in the study and after the treatment with Seroquel XR for 8 weeks.
PLEASE NOTE: Seroquel SR and Seroquel XR refer to the same formulation. The SR designation was changed to XR after consultation with FDA.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adult patients with Schizophrenia prescribed on Seroquel XR according to the approved product information before inclusion in this non-interventional study
- •Signed and dated Patient Informed Consent (ICF)
排除标准
- •Hypersensitivity to the active substance or to any of the excipients of Seroquel XR
结局指标
主要结局
Improvement in CGI scores and BPRS comparing visits 1 and 3.
时间窗: twice with 4 week interval
次要结局
- To evaluate compliance to therapy(twice with 4 week interval)
研究者
研究点 (2)
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