Study of Aripiprazole to Reduce Medical Risks in Bipolar Disorder

NATerminatedINTERVENTIONAL
Enrollment

3

Participants

Timeline

Start Date

April 30, 2008

Primary Completion Date

August 31, 2009

Study Completion Date

August 31, 2009

Conditions
Bipolar DisorderMetabolic Syndrome
Interventions
DRUG

Aripiprazole

All subjects will be assessed at baseline and then switched from their current antimanic agent to aripiprazole. Arpipirazole will be titrated from a starting dose of 5 mg/day up to a target dose of 15 mg/day over a period of up to 2 months (approximately 8 weeks). Concomitant medication will not be changed unless medically necessary. If a subject is taking an antipsychotic in addition to divalproex, aripiprazole will replace the antipsychotic.

Trial Locations (1)

15213

University of Pittsburgh Medical Center, Pittsburgh

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

lead

University of Pittsburgh

OTHER

NCT00665444 - Study of Aripiprazole to Reduce Medical Risks in Bipolar Disorder | Biotech Hunter | Biotech Hunter