NCT00042029已完成3 期
A Double-Blind, Multicenter, Placebo-Controlled Study of MK0869 in the Treatment of Patients With Major Depressive Disorder
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 324
- 主要终点
- HAMD-17 total score; Tolerability
研究概览
简要总结
A clinical study to determine the efficacy and safety of MK0869 in the treatment of depression.
详细描述
The duration of treatment is 8 weeks.
研究设计
- 研究类型
- Interventional
- 主要目的
- Treatment
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
- •Patients with Major Depressive Disorder
排除标准
- 未提供
结局指标
主要结局
HAMD-17 total score; Tolerability
次要结局
- CGI-I Scale score; Sheehan Disability Scale
研究者
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