drugset / Trial / NCT00282464
A Six-week Flexible Dose Study Evaluating the Efficacy and Safety of Geodon in Patients With Bipolar I Depression.
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a 6-week trial that evaluates the efficacy and safety of Geodon (ziprasidone) in outpatient subjects ages 18 and older with Bipolar Disorder type I, depressed. Subjects are required to undergo a washout period of at least 7 days of any prior med.
Timeline
- Start
- 2006-02
- Primary completion
- 2008-03
- Completion
- 2008-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Ziprasidone | Small molecule | 20 mg | Oral |
| Comparator | Ziprasidone | Small molecule | 40 mg | Oral |
| Comparator | Ziprasidone | Small molecule | 60 mg | Oral |
| Comparator | Ziprasidone | Small molecule | 80 mg | Oral |