CompletedNCT00282464
A Six-week Flexible Dose Study Evaluating the Efficacy and Safety of Geodon in Patients With Bipolar I Depression.
Medication studyAges 18+United StatesBipolarity
Understand this study
Who was this study for?
Listed age limits: from 18 years.
- Listed locations
- Dothan and 42 more locationsSee all locations and recruitment
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study information
Study start dateFebruary 2006
- Recruitment status
- Completed
- Enrollment listed in the registry
- 392
- Sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
- Sponsor type
- Other organization
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
- Locations
- United States
- Age range
- Over 18 Years
- Official registry ID
- NCT00282464
- Official title
Show the full official title
A Six-Week, Double-Blind, Multicenter, Placebo-Controlled Study Evaluating the Efficacy and Safety of Flexible Doses of Oral Ziprasidone in Outpatients With Bipolar I Depression
Recruitment & locations
CompletedDothan · Little Rock · Anaheim
39 more locations
- Cerritos
- Chula Vista
- Escondido
- Los Angeles
- Riverside
- San Diego
- Santa Ana
- Denver
- Darien
- Boca Raton
- Bradenton
- Jacksonville
- Melbourne
- Orange City
- Tampa
- Atlanta
- Marietta
- Eagle
- Granite City
- Terre Haute
- Glen Burnie
- Towson
- Rochester
- St Louis
- Princeton
- Brooklyn
- New York
- Olean
- Durham
- Raleigh
- Toledo
- Tulsa
- Philadelphia
- Scranton
- Lincoln
- Dallas
- Houston
- San Antonio
- Charlottesville
Questions about this study
Who is behind this study?
The study sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Did this study involve medication?
Yes. The study involved medication, including Placebo and Geodon (Ziprasidone).
Who was this study for?
Listed age limits: from 18 years.
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