Efficacy and Safety With Ziprasidone in First-episode Psychosis

NCT ID: NCT01157559

Last Updated: 2010-07-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

27 participants

Study Classification

INTERVENTIONAL

Study Completion Date

2010-05-31

Brief Summary

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The aim of the study is to investigate the efficacy and safety of ziprasidone in patients with first episode psychosis.

Detailed Description

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Conditions

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First Episode Psychosis

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Ziprasidone

8 week prospective study

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients who meet DSM-IV criteria for first episode schizophrenia, schizophreniform disorder and schizoaffective disorder

Exclusion Criteria

* Patients with previously prescribed antipsychotic medication in 2 weeks or more
* patients with substance-induced psychotic disorder, serious suicide attempt, neurological disorder, etc.
Minimum Eligible Age

14 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role collaborator

Chonbuk National University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Chonbuk National University Hospital, Jeonju, Korea

Locations

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Department of Psychiatry, Chonbuk national University Hospital

Jeonju, , South Korea

Site Status

Heo psychiatric Hospital

Jeonju, , South Korea

Site Status

Jeonju Jesus Hospital

Jeonju, , South Korea

Site Status

Countries

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South Korea

Other Identifiers

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2006-Zeldox in FEP

Identifier Type: -

Identifier Source: org_study_id

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