Columbia University Medical Center
NewYork-Presbyterian Hospital The University Hospital of Columbia and Cornell

brain activity measurement before and after antidepressant treatment

Please refer to this study by identifier 6/10/2011

Principal Investigator(s)

Gerard Bruder

Purpose

This study compares outcomes of treatment for depression with two standard anti-depressant medicines that work differently in the body. Several brain tests performed prior to and after treatment at week 1 and week 12 intervals will be performed to ascertain brain differences associated with depression and to determine whether these test results change during treatment or predict treatment response.

  • Type of Study: Clinical Trial
  • Setting of Study: outpatient
  • Clinical Trials.gov number: 
  • Providing Clinical Treatment?: Yes
  • No Cost Treatment?: Yes
  • Care is provided in languages: English

Study Activities

  • Filling Out Forms
  • Computer Tasks
  • Blood Samples
  • Psychophysiology measurements
  • Provides Payment: Compensation for study related procedures

Eligibility

  • Ages Eligible for Study: 18 Years - 65 Years
  • Genders Eligible for Study: Both
  • This study is recruiting Healthy Volunteers.

Criteria

  • Inclusion Criteria:
    Patients
    1) diagnosis of major depression, dysthymia or depression NOS
    2) 18-65 years old
    3) male or female

    Normal Controls
    1) 18-65 years old
    2) male or female
  • Links
    Depression Evaluation Service website
    Columbia Department of Psychiatry
    New York State Psychiatric Institute
  • Location: Unit 50 NYSPI 1051 Riverside Drive New York, NY 10032
  • Clinic: Depression Evaluation Service
  • Division: Therapeutics
  • Study chairs or principal investigators: Gerard Bruder PhD, Principal Investigator
  • Co-investigators: Jonathan Stewart, Craig Tenke, Jergen Kayser, Jeff Miller, Ronit Kishon

For more information, please contact

Gerard Bruder

Tel: 212-543-5468

E-mail: bruderg@nyspi.columbia.edu


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