Trial Information
Summary: SSRI Versus Bupropion in High-Risk Major Depressive Disorder
The Department of Neuroscience at the New York State Psychiatric
Institute is conducting a research study on the prevention of
suicidal behavior in Major Depressive Disorder using medications,
and is looking for people interested in participating. The goal of
our study is to compare the effect of Wellbutrin (bupropion) versus
Paxil (paroxetine) on the vulnerability to suicidal behavior during
a 6-month period following a Major Depressive Episode. Both
Wellbutrin and Paxil are antidepressants which have been approved
by the Food and Drug Administration (FDA) for the treatment of
Major Depressive Disorder.
We are offering free outpatient medication monitoring visits at
the Neuroscience Clinic for a period of 6 months.
If you are interested, or have a family member who is suffering
from Major Depressive Disorder, and would like further information,
please call.
Inclusion Criteria
- Between 18 and 75 years old
- Currently in a Major Depressive Episode
- History of a past suicide attempt or current suicidal
ideation
- Must live within the New York City metro area, since patients
are required to come in regularly for psychopharmacological
treatment visits
Exclusion Criteria
- History of Bipolar Disorder
- Contraindication to Paxil or Wellbutrin
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Contact:
Lucia Sanchez-Diaz, B.A.
New York State Psychiatric Institute
Department of Neuroscience
1051 Riverside Drive Unit 42
New York, NY 10032
Telephone: 212-543-6216
Fax: 212-543-2958
Email:
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Trial listings updated: June 1, 2008 at 6:31:44 AM