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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00422331
Other study ID # JDS04004
Secondary ID Lithium TEAM-1 S
Status Active, not recruiting
Phase Phase 3
First received January 11, 2007
Last updated August 13, 2007
Start date January 2007
Est. completion date December 2007

Study information

Verified date August 2007
Source JDS Pharmaceuticals
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug AdministrationIndia: Ministry of Health
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Lithium Carbonate Capsule


Locations

Country Name City State
United States JDS Pharmaceuticals New York New York

Sponsors (1)

Lead Sponsor Collaborator
JDS Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

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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