Trial Information
Summary: Pharmacotherapy of High-Risk Bipolar Disorder
The Department of Neuroscience at the New York State Psychiatric
Institute is conducting a research study on the prevention of
suicidal behavior in Bipolar Disorder using medications, and is
looking for people interested in participating. The goal of our
study is to compare the effect of Lithium versus Depakote
(valproate) on the vulnerability to suicidal behavior during a
24-month period following either a Major Depressive Episode or a
Mixed Episode. Both Lithium and Depakote are mood stabilizers which
have been approved by the Food and Drug Administration (FDA) for
the treatment of Bipolar Disorder. We are offering free outpatient
medication monitoring visits at the Neuroscience Clinic for a
period of up to 24 months.
If you are interested, or have a family member who is suffering
from Bipolar Disorder, and would like further information, please
call Lucia at 212-543-6216.
Partial Inclusion Criteria:
- Between 18 and 75 years old
- Currently in a Major Depressive or Mixed Episode
- History of a past suicide attempt
- Must live within the New York City metro area, since patients
are required to come in regularly for psychopharmacological
treatment visits
Partial Exclusion Criteria
- Requires detoxification from alcohol or other substances
- Responded poorly to Lithium or Depakote in the past
For more information,
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Contact:
Lucia Sanchez-Diaz, Research Coordinator
New York State Psychiatric Institute
Department of Neuroscience
Box 42 1051 Riverside Drive
New York, NY 10032
Telephone: 212-543-6216
Fax: 212-543-6017
Email:
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Trial listings updated: June 1, 2008 at 5:44:56 AM