NCT00036335已完成3 期
Duloxetine Hydrochloride (LY248686) Protocol F1J-US-HMCB Duloxetine Once-Daily Dosing Versus Placebo in Patients With Major Depression and Pain
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 286
- 试验地点
- 25
研究概览
简要总结
The purposes of this study are to determine whether an investigational drug can help patients suffering from major depression with pain symptoms, and gather data on the safety of the investigational drug including any side effects that might be associated with it.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •You must be suffering from symptoms of depression for at least the past 2 weeks (sadness, loss of interest in daily activities, feelings of hopelessness or guilt, sleeplessness or lack of energy)
- •You must have pain symptoms with no known cause, such as unexplainable, head, chest, or back pain, overall aches and pains, or other unexplainable pains.
- •You need to be available to visit a doctor's office about once a week for 10 weeks.
排除标准
- •You are a woman and are pregnant or breastfeeding.
- •You have a current or previous diagnosis of bipolar disorder, schizophrenia, or other psychotic disorder.
- •You have had a primary diagnosis of an anxiety disorder within the past 6 months.
- •You have a history of alcohol or drug dependence or abuse within the past 6 months.
- •You have a serious medical illness.
研究者
研究点 (25)
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