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临床试验/NCT00260182
NCT00260182
已完成
不适用

Genetics of Recurrent Early Onset Major Depression

Stanford University6 个研究点 分布在 1 个国家目标入组 2,302 人开始时间: 2005年10月最近更新:
适应症Depression

概览

阶段
不适用
状态
已完成
入组人数
2,302
试验地点
6
主要终点
Major depressive disorder diagnosis

概览

简要总结

This study will identify specific genes that may cause a predisposition to depression in some families.

详细描述

Depression is a serious medical illness that is often difficult to diagnose and treat. Studies on patterns of depression within families suggest that inherited genes may cause a predisposition to the disorder. People with early onset depression often have more relatives with depression than people whose depression does not begin until later in life. It is likely that several interacting genes cause this tendency towards the disorder, rather than one specific gene. This study will serve to identify particular genes that may cause a susceptibility to depression in order to better understand the brain mechanisms involved with severe depression. In turn, this may aid in the development of new treatments for depression.

Participation in this observational study will entail one interview and one blood test. Participants will be interviewed, either in person or by telephone, about their personal and family psychiatric history. The blood sample will be collected at a time and location that is convenient for the participant. Participants may also be asked to invite other family members to participate in the study.

For information on a related study please follow this link:

http://clinicaltrials.gov/show/NCT00005914

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
21 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • History of recurrent major depression
  • Has a parent or sibling with a history of recurrent major depression
  • Depression began before the age of 31

排除标准

  • Bipolar I (manic-depressive) disorder
  • Schizophrenia

结局指标

主要结局

Major depressive disorder diagnosis

时间窗: One patient interview session (typically 2 hours), and blood draw (10-20 minutes)

The study will correlate genome-wide SNP genotypes with case vs. control status, defined by presence or absence of major depressive disorder. Participants will attend an interview regarding personal and family history of psychiatric disorders, and give a blood specimen. Genotypes from blood samples will be studied for association with presence of major depressive disorder.

次要结局

未报告次要终点

研究者

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

Douglas F. Levinson

Principle Investigator

Stanford University

研究点 (6)

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