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临床试验/NCT00817011
NCT00817011Unknown不适用

Phase 4 Study of Development of Pharmacogenomic Method to Predict Antidepressant Responsiveness

Samsung Medical Center1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2006年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
1,000
试验地点
1
主要终点
all pharmacogenetic and biological marker variables cause drug response

研究概览

简要总结

The Purpose of this study is to predict antidepressant response in advance using pharmacogenomics and peripheral biological markers in depressed patients.

详细描述

The difficulties to treat depressed patients are 1)the patients don't respond to antidepressant is about 40% of which, and 2) The time lag is existed until the patients respond to antidepressant and show the treatment effects.

If it is predicted the response of antidepressant in advance, it would be overcome such problems. Drug response generally is known to be related to the individual genetic information and the environmental factors. We are going to investigation about antidepressant response using these approaches.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
25 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 25 < age <85
  • major depressed patients satisfied with the diagnosis criteria depression of DSM-IV
  • interview with one more patient's family member for objective diagnosis and final diagnosis decision by agreements of two more psychiatric physicians

排除标准

  • received psychotropic medication within 2 weeks of the study or fluoxetine within 4 weeks
  • potential study participants for pregnancy, significant medical conditions, abnormal laboratory baseline values, unstable psychiatric features(eg.suicidal), history of alcohol of drug dependence, seizures, head trauma with loss of consciousness, neurological illness, or concomitant Axis I psychiatric disorder.

研究组 & 干预措施

SSRI treated group

Experimental

SSRI treated group are depressive patients treated with fluoxetine, paroxetine, citalopram or sertraline

干预措施: SSRI treated group (Drug)

non-SSRI treated group

Active Comparator

non-SSRI treated group are depressive patients treated with venlafaxine, nortriptyline, bupropion, duloxetine, trazodone or mirtazapine

干预措施: non-SSRI treated group (Drug)

结局指标

主要结局

all pharmacogenetic and biological marker variables cause drug response

时间窗: 24weeks

次要结局

  • all clinical cause drug response(24weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Doh Kwan Kim

M.D., Ph.D

Samsung Medical Center

研究点 (1)

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