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Completed Phase 3 Interventional Results available

A Six-week Flexible Dose Study Evaluating the Efficacy and Safety of Geodon in Patients With Bipolar I Depression.

ClinicalTrials.gov ID: NCT00282464

Public ClinicalTrials.gov record NCT00282464. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 8:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00282464
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
392 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2006 (Type not available)
Primary completion
Mar 2008 (Actual)
Completion
Mar 2008 (Actual)
Last update posted
Mar 29, 2021

2006 – 2008

United States locations

U.S. sites
43
U.S. states
22
U.S. cities
42
Facility City State ZIP Site status
Pfizer Investigational Site Dothan Alabama 36303 —
Pfizer Investigational Site Little Rock Arkansas 77205 —
Pfizer Investigational Site Anaheim California 92804 —
Pfizer Investigational Site Cerritos California 90703 —
Pfizer Investigational Site Chula Vista California 91910 —
Pfizer Investigational Site Escondido California 92025 —
Pfizer Investigational Site Los Angeles California 90027-5302 —
Pfizer Investigational Site Riverside California 92506 —
Pfizer Investigational Site San Diego California 92126 —
Pfizer Investigational Site Santa Ana California 92705 —
Pfizer Investigational Site Denver Colorado 80220 —
Pfizer Investigational Site Darien Connecticut 06820 —
Pfizer Investigational Site Boca Raton Florida 33432 —
Pfizer Investigational Site Bradenton Florida 34208 —
Pfizer Investigational Site Jacksonville Florida 32256-2006 —
Pfizer Investigational Site Melbourne Florida 32901 —
Pfizer Investigational Site Orange City Florida 32763 —
Pfizer Investigational Site Tampa Florida 33613 —
Pfizer Investigational Site Atlanta Georgia 30328 —
Pfizer Investigational Site Marietta Georgia 30060 —
Pfizer Investigational Site Eagle Idaho 83616 —
Pfizer Investigational Site Granite City Illinois 62040-4749 —
Pfizer Investigational Site Terre Haute Indiana 47802 —
Pfizer Investigational Site Glen Burnie Maryland 21061 —
Pfizer Investigational Site Towson Maryland 21204 —
Pfizer Investigational Site Rochester Minnesota 55905 —
Pfizer Investigational Site St Louis Missouri 63118 —
Pfizer Investigational Site Princeton New Jersey 08540 —
Pfizer Investigational Site Brooklyn New York 11223 —
Pfizer Investigational Site Brooklyn New York 11235 —
Pfizer Investigational Site New York New York 10003 —
Pfizer Investigational Site Olean New York 14760 —
Pfizer Investigational Site Durham North Carolina 27704 —
Pfizer Investigational Site Raleigh North Carolina 27609 —
Pfizer Investigational Site Toledo Ohio 43623 —
Pfizer Investigational Site Tulsa Oklahoma 74135 —
Pfizer Investigational Site Philadelphia Pennsylvania 19149 —
Pfizer Investigational Site Scranton Pennsylvania 18503 —
Pfizer Investigational Site Lincoln Rhode Island 02865 —
Pfizer Investigational Site Dallas Texas 75231 —
Pfizer Investigational Site Houston Texas 77007 —
Pfizer Investigational Site San Antonio Texas 78229 —
Pfizer Investigational Site Charlottesville Virginia 22903-4895 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00282464, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 29, 2021 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00282464 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →