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临床试验/NCT00045773
NCT00045773已完成不适用

Treatment Outcome of Vascular Depression

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 208 人开始时间: 2001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
状态
已完成
入组人数
208
试验地点
2

研究概览

简要总结

This 12-week study will evaluate the effectiveness of sertraline (Zoloft®) for treatment of depression associated with small vascular lesions in the brain (vascular depression).

详细描述

Major late life depression (LLD) is an important health problem with a large and growing number of affected individuals. A significant subset of patients with LLD, particularly those with vascular depression, have abnormalities in certain parts of the brain that are evident on MRI scans and may be associated with poor acute and long-term response to antidepressant treatment. Studies have also indicated that LLD patients frequently have frontal lobe dysfunction. A longitudinal study with the antidepressant nortriptyline has demonstrated that frontal lobe dysfunction is associated with poor acute response and a greater risk for recurrence of LLD. However, it is not known if this finding applies to other antidepressants. This study will be the first clinical trial to simultaneously test the effects of specific brain and psychological factors on course of response, remission rate, and other measures of health outcomes in people with LLD.

Participants are treated with sertraline for 12 weeks. During this period, participants undergo cognitive testing, MRI, electrocardiogram (EKG), and laboratory tests. Study visits occur every 2 weeks.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • DSM-IV criteria for MDD
  • Hamilton Depression Rating Scale score >18
  • No MRI contraindications, e.g. foreign metallic implants, pacemaker
  • Medication free of any psychotropic drug except as otherwise noted for set washout period (see D.2.1)
  • Mini Mental Status Exam score <21
  • No unstable medical disorders (requiring immediate medical attention)
  • Ability to give informed consent
  • English speaking

排除标准

  • Does not meet DSM-IV criteria for MDD
  • Hamilton Depression Rating Scale score <18
  • MRI contraindications e.g. foreign metallic implants, pacemaker
  • Psychotropic drug use other than zolpidem and lorazepam, prn within 2 weeks of entry
  • Mini Mental Status Exam score >21, or known primary neurological disorders including Dementia of the Alzheimer type, Parkinson's Disease, multiple sclerosis, seizure disorder.
  • Unstable medical disorders, uncorrected hypothyroidism, or any condition that in the investigators opinion makes the patients unsuitable for a trial
  • Cannot give informed consent
  • Does not speak English

研究组 & 干预措施

1

干预措施: Sertraline (Drug)

研究者

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

Yvette Sheline

Penn Faculty - McLure Professor

University of Pennsylvania

研究点 (2)

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