Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00097266
Other study ID # CN138-162
Secondary ID
Status Completed
Phase Phase 3
First received November 19, 2004
Last updated November 7, 2013
Start date December 2004
Est. completion date January 2007

Study information

Verified date July 2010
Source Otsuka Pharmaceutical Development & Commercialization, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to confirm the safety and effectiveness of aripiprazole therapy over 12 weeks in subjects with bipolar disorder experiencing symptoms of mania.


Recruitment information / eligibility

Status Completed
Enrollment 615
Est. completion date January 2007
Est. primary completion date January 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subjects with Bipolar I Disorder and a diagnosis of acute mania will be considered for this study.

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:
Placebo
Tablets/capsules, oral, 0 mg, once daily, 3 weeks (switched to arm B for an additional 9 weeks).
Aripiprazole
Tablets, oral, 15-30 mg, once daily, 12 weeks.
Haloperidol
Capsule, oral, 5-15 mg, once daily, 12 weeks.

Locations

Country Name City State
Bulgaria Local Institution Burgas
Bulgaria Local Institution Novi Iskar
Bulgaria Local Institution Pleven
Bulgaria Local Institution Sofia
Bulgaria Local Institution Varna
Croatia Local Institution Osijek
Croatia Local Institution Rijeka
Croatia Local Institution Split
Croatia Local Institution Zagreb
Mexico Local Institution Col. Obispado Nuevo Leon
Mexico Local Institution Fracc. Industrias San Luis Potosi
Mexico Local Institution Merida Yucatan
Mexico Local Institution Mexico Distrito Federal
Mexico Local Institution Monterrey Nuevo Leon
Mexico Local Institution Nuevo Leon
Mexico Local Institution Zapopan Jalisco
Peru Local Institution Lima
Russian Federation Local Institution Arkhangelsk
Russian Federation Local Institution Kazan
Russian Federation Local Institution Leningrad Region
Russian Federation Local Institution Lipetsk Lipetsk Region
Russian Federation Local Institution Moscow
Russian Federation Local Institution Nizhniy Novgorod
Russian Federation Local Institution Samara
Russian Federation Local Institution St. Petersburg
Russian Federation Local Institution Volgograd
South Africa Local Institution Berea Kwa Zuluu Natal
South Africa Local Institution Durban Kwa Zulu Natal
South Africa Local Institution Florida Gauteng
South Africa Local Institution Pretoria Gauteng
United States Local Institution Albuquerque New Mexico
United States Local Institution Anaheim California
United States Local Institution Cerritos California
United States Local Institution Cleveland Ohio
United States Local Institution Desoto Texas
United States Local Institution Garden Grove California
United States Local Institution Maitland Florida
United States Local Institution National City California
United States Local Institution Oklahoma City Oklahoma
United States Local Institution Pico Rivera California
United States Local Institution Riverside California
United States Local Institution San Diego California
United States Local Institution Shreveport Louisiana
United States Local Institution Tampa Florida
United States Local Institution Washington District of Columbia

Sponsors (2)

Lead Sponsor Collaborator
Otsuka Pharmaceutical Development & Commercialization, Inc. Otsuka America Pharmaceutical

Countries where clinical trial is conducted

United States,  Bulgaria,  Croatia,  Mexico,  Peru,  Russian Federation,  South Africa, 

References & Publications (1)

Young AH, Oren DA, Lowy A, McQuade RD, Marcus RN, Carson WH, Spiller NH, Torbeyns AF, Sanchez R. Aripiprazole monotherapy in acute mania: 12-week randomised placebo- and haloperidol-controlled study. Br J Psychiatry. 2009 Jan;194(1):40-8. doi: 10.1192/bjp.bp.108.049965. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in a mania rating scale at endpoint
Secondary Response rate and Clinical Global Impression scale at endpoint
See also
  Status Clinical Trial Phase
Completed NCT05111548 - Brain Stimulation and Cognitive Training - Efficacy N/A
Completed NCT02855762 - Targeting the Microbiome to Improve Clinical Outcomes in Bipolar Disorder N/A
Recruiting NCT05915013 - Alpha-Amino-3-Hydroxy-5-Methyl-4- Isoxazole Propionic Acid Receptor Components of the Anti-Depressant Ketamine Response Phase 1
Recruiting NCT05206747 - Ottawa Sunglasses at Night for Mania Study N/A
Completed NCT02513654 - Pharmacokinetics, Safety and Tolerability of Repeat Dosing Lamotrigine in Healthy Chinese Subjects Phase 1
Recruiting NCT06313918 - Exercise Therapy in Mental Disorders-study N/A
Completed NCT02304432 - Targeting a Genetic Mutation in Glycine Metabolism With D-cycloserine Early Phase 1
Recruiting NCT06197048 - Effect of Nutritional Counseling on Anthropometry and Biomarkers in Patients Diagnosed With Schizophrenia/Psychosis or Bipolar Affective Disorder N/A
Completed NCT03497663 - VIA Family - Family Based Early Intervention Versus Treatment as Usual N/A
Completed NCT04284813 - Families With Substance Use and Psychosis: A Pilot Study N/A
Completed NCT02212041 - Electronic Cigarettes in Smokers With Mental Illness N/A
Recruiting NCT05030272 - Comparing Two Behavioral Approaches to Quitting Smoking in Mental Health Settings N/A
Recruiting NCT04298450 - ED to EPI: Using SMS to Improve the Transition From the Emergency Department to Early Psychosis Intervention N/A
Active, not recruiting NCT03641300 - Efficacy of Convulsive Therapies for Bipolar Depression N/A
Not yet recruiting NCT04432116 - Time and Virtual Reality in Schizophrenia and Bipolar Disorder N/A
Terminated NCT02893371 - Longitudinal Comparative Effectiveness of Bipolar Disorder Therapies
Completed NCT02970721 - Use of Psychotropic Medications Among Pregnant Women With Bipolar Disorder
Terminated NCT02909504 - Gao NARASD Lithium Study Phase 4
Recruiting NCT03088657 - Design and Methods of the Mood Disorder Cohort Research Consortium (MDCRC) Study
Recruiting NCT02481245 - BezafibrateTreatment for Bipolar Depression: A Proof of Concept Study Phase 2