Bipolar Disorder Clinical Trial
Official title:
Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Multicenter, Efficacy and Safety Study of Lithium in Bipolar I Disorder
The purpose of this study is to determine whether Lithium is safe and effective in the treatment of Bipolar I Disorder subjects with symptoms of acute mania.
Status | Active, not recruiting |
Enrollment | 206 |
Est. completion date | December 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Diagnosis of Bipolar 1 Disorder; - Hospitalized or in the process of being hospitalized for a manic or mixed episode Exclusion Criteria: - History of rapid cycling; - History of hypersensitivity or adverse reaction to lithium |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | JDS Pharmaceuticals | New York | New York |
Lead Sponsor | Collaborator |
---|---|
JDS Pharmaceuticals |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change from baseline in YMRS score | |||
Secondary | change from baseline in CGI-BP score | |||
Secondary | change from baseline in MADRS score |
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