NCT00042575已完成3 期
Protocol F1J-US-HMBY Dose Escalation, Double-Blind Treatment With Duloxetine Hydrochloride Once Daily Dosing for Evaluation of Safety in Major Depression
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 120
- 试验地点
- 9
研究概览
简要总结
The Purposes of this Study are to determine:
The safety of duloxetine and any side effects that might be associated with it.
Whether duloxetine can help patients with major depression.
It is possible that information collected during this study will be analyzed by the sponsor in the future to evaluate duloxetine for other possible uses or for other medical or scientific purposes other than those currently proposed.
Duloxetine might not have any good effects for you.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •You must be at least 18 years old.
- •You must be diagnosed with major depressive disorder
- •You must be able to visit the doctor's office once a week to once every 2 weeks for a total of 8 weeks.
排除标准
- •You are a woman and are pregnant or breastfeeding.
- •You have a current or previous major psychiatric disorder other than depression, such as bipolar disorder, schizophrenia, or other psychotic disorder.
- •You have a history of alcohol or drug dependence or abuse within the past 6 months.
- •You are allergic to the study drug or you have experienced allergic reactions when taking several medications at once.
- •You have a serious medical illness.
研究者
研究点 (9)
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