Functional Change and Efficacy of Duloxetine in Patients With Co-Morbid Depression & Soft Tissue Discomfort Syndrome
Functional Change and Efficacy of Duloxetine in Patients With Major Depression and Co-Morbid Soft Tissue Discomfort Symptoms
The objective of this study is to determine the time course of duloxetine efficacy on the symptoms of Major Depressive Disorder (MDD)and on the symptoms of Soft Tissue Discomfort Syndrome(STDS) via use of 24-hour Actigraph™ measures.
We hypothesize that there will be a reduction in both MDD and STDS symptoms in MDD patients with co-morbid STDS symptoms. We further hypothesize that there will be a rapid improvement in functional outcome ratings and 24-hour activity in MDD patients with co-morbid STDS symptoms which may occur even before the antidepressant effect is observed.
研究概览
研究类型
注册 (实际的)
阶段
- 第四阶段
联系人和位置
学习地点
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Pennsylvania
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Philadelphia、Pennsylvania、美国、19104-3309
- Depression Research Unit, University of Pennsylvania School of Medicine
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- > 17 years old
- All races and ethnicity
- DSM IV-TR Axis I diagnosis of MDD
- Co-morbid STDS
- Baseline 17-item Hamilton Depression Rating > 13
Exclusion Criteria:
- Primary Axis I disorder other than MDD
- History of mania or psychosis
- Actively suicidal
- Required hospitalization
- A alcohol or substance abuse or dependence within the preceding 3 months
- Pregnant or nursing
- Unstable medical condition (other than STDS)
- Narrow-angle glaucoma
- Sensitivity to duloxetine, concurrent antidepressant, tranquilizer, or mood stabilizer use
- Hepatic or renal insufficiency
学习计划
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：不适用
- 介入模型：单组作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：度洛西汀
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30-60 mg daily for 8 weeks
其他名称：
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研究衡量的是什么？
主要结果指标
结果测量 |
大体时间 |
|---|---|
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24-hour Activity Level
大体时间：Baseline and Week One of Treatment
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Baseline and Week One of Treatment
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Functional Symptom Questionnaire
大体时间：Baseline; Week 6 and Week 8 of Treatment
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Baseline; Week 6 and Week 8 of Treatment
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合作者和调查者
调查人员
- 首席研究员：Jay D Amsterdam, MD、University of Pennsylvania
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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