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Study of Aripiprazole in the Treatment of Patients with Acute Symptoms in Bipolar Disorder - Article


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Aripiprazole

Abilify


Clinical Trial: Study of Aripiprazole in the Treatment of Patients with Acute Symptoms in Bipolar Disorder

This study is no longer recruiting patients.

Sponsored by: Bristol-Myers Squibb
Information provided by: Bristol-Myers Squibb

Purpose

The purpose of this study is to learn if aripiprazole is effective for the treatment of patients with acute symptoms of Bipolar disorder.

Condition Treatment or Intervention Phase
Bipolar Disorder
 Drug: aripiprazole
Phase III

MedlinePlus related topics:  Bipolar Disorder

Study Type: Interventional
Study Design: Treatment

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

Patients with acute symptoms of Bipolar Disorder


Location Information


Alabama
      Local Institution, Tuscaloosa,  Alabama,  United States

Arizona
      Local Institution, Little Rock,  Arizona,  United States

California
      Local Institution, Chula Vista,  California,  United States

      Local Institution, Beachwood,  California,  United States

      Local Institution, San Clemente,  California,  United States

      Local Institution, Stanford,  California,  United States

      Local Institution, San Diego,  California,  United States

      Local Institution, Riverside,  California,  United States

      Local Institution, San Diego,  California,  United States

District of Columbia
      Local Institution, Washington,  District of Columbia,  United States

Florida
      Local Institution, Winter Park,  Florida,  United States

      Local Institution, North Miami,  Florida,  United States

Hawaii
      Local Institution, Honolulu,  Hawaii,  United States

Illinois
      Local Institution, Chicago,  Illinois,  United States

Indiana
      Local Institution, Indianapolis,  Indiana,  United States

Kentucky
      Local Institution, Louisville,  Kentucky,  United States

Massachusetts
      Local Institution, Belmont,  Massachusetts,  United States

      Local Institution, Newton Center,  Massachusetts,  United States

Michigan
      Local Institution, New Baltimore,  Michigan,  United States

New York
      Local Institution, Lawrence,  New York,  United States

North Carolina
      Local Institution, Butner,  North Carolina,  United States

Ohio
      Local Institution, Cincinnati,  Ohio,  United States

      Local Institution, Medina,  Ohio,  United States

      Local Institution, Cincinnati,  Ohio,  United States

Pennsylvania
      Local Institution, Philadelphia,  Pennsylvania,  United States

Texas
      Local Institution, Austin,  Texas,  United States

      Local Institution, Houston,  Texas,  United States

      Local Institution, Houston,  Texas,  United States

Virginia
      Local Institution, Falls Church,  Virginia,  United States

Washington
      Local Institution, Bellevue,  Washington,  United States

More Information

Study ID Numbers:  CN138-074
Record last reviewed:  February 2004
Last Updated:  October 13, 2004
Record first received:  May 7, 2002
ClinicalTrials.gov Identifier:  NCT00036101
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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September 6, 2008



Page Updated: September 6, 2005
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