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Study of Aripiprazole in Patients With a History of Bipolar Disorder
This study has been completed.
Sponsored by: Bristol-Myers Squibb
Information provided by: Bristol-Myers Squibb
ClinicalTrials.gov Identifier: NCT00036348
  Purpose

The purpose of this study is to learn if aripiprazole is effective in the treatment of patients with a history of bipolar disorder.


Condition Intervention Phase
Bipolar Disorder
Drug: Aripiprazole
Phase III

MedlinePlus related topics: Bipolar Disorder
Drug Information available for: Aripiprazole
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Patients with a history of Bipolar I Disorder

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00036348

Locations
United States, Alabama
Local Institution
Birmingham, Alabama, United States
Local Institution
Tuscaloosa, Alabama, United States
United States, California
Local Institution
Chillicothe, California, United States
Local Institution
Riverside, California, United States
Local Institution
Torrance, California, United States
Local Institution
Stanford, California, United States
United States, Georgia
Local Institution
Atlanta, Georgia, United States
United States, Illinois
Local Institution
Chicago, Illinois, United States
United States, Kentucky
Local Institution
Louisville, Kentucky, United States
United States, Louisiana
Local Institution
Shreveport, Louisiana, United States
United States, Massachusetts
Local Institution
Belmont, Massachusetts, United States
United States, Nevada
Local Institution
Las Vegas, Nevada, United States
United States, New Mexico
Local Institution
Albuquerque, New Mexico, United States
United States, New York
Local Institution
New York, New York, United States
United States, Pennsylvania
Local Institution
Philadelphia, Pennsylvania, United States
United States, Tennessee
Local Institution
Memphis, Tennessee, United States
Local Institution
Nashville, Tennessee, United States
United States, Texas
Local Institution
San Antonio, Texas, United States
Local Institution
Austin, Texas, United States
Sponsors and Collaborators
Bristol-Myers Squibb
  More Information

BMS Clinical Trials Disclosure  This link exits the ClinicalTrials.gov site
For FDA Safety Alerts and Recalls refer to the following link www.fda.gov/MEDWATCH/safety.htm  This link exits the ClinicalTrials.gov site

Publications indexed to this study:
Study ID Numbers: CN138-010
Study First Received: May 8, 2002
Last Updated: June 27, 2008
ClinicalTrials.gov Identifier: NCT00036348  
Health Authority: United States: Food and Drug Administration

Keywords provided by Bristol-Myers Squibb:
Bipolar I disorder

Study placed in the following topic categories:
Affective Disorders, Psychotic
Mental Disorders
Bipolar Disorder
Mood Disorders
Psychotic Disorders
Aripiprazole

Additional relevant MeSH terms:
Tranquilizing Agents
Pathologic Processes
Disease
Therapeutic Uses
Physiological Effects of Drugs
Psychotropic Drugs
Central Nervous System Depressants
Antipsychotic Agents
Central Nervous System Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009