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Safety and Efficacy of Ziprasidone in Adolescents With Schizophrenia - Article


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Tetracycline Tablets or Capsules

Achromycin; Sumycin Capsules; TCN; Tetracycline Hydrochloride; Wesmycin 




Clinical Trial: Safety and Efficacy of Ziprasidone in Adolescents With Schizophrenia

This study is not yet open for patient recruitment.
Verified by Pfizer January 2006

Sponsored by: Pfizer
Information provided by: Pfizer
ClinicalTrials.gov Identifier: NCT00257192

Purpose

The purpose of this study is to determine if flexibly-dosed ziprasidone is safe and effective for the treatment of adolescents (ages 13-17) with schizophrenia
Condition Intervention Phase
Schizophrenia
 Drug: Ziprasidone oral capsules
Phase III

MedlinePlus related topics:  Schizophrenia

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Official Title: Six Week, Double-Blind, Placebo Controlled Phase III Trial Evaluating The Efficacy, Safety And Pharmacokinetics Of Flexible Doses Of Oral Ziprasidone In Adolescent Subjects With Schizophrenia

Further study details as provided by Pfizer:
Primary Outcomes: Brief Psychiatric Rating Scale - Anchored
Secondary Outcomes: Positive and Negative Syndrome Scale; Clinical Global Impression scale
Expected Total Enrollment:  276

Study start: January 2006

Eligibility

Ages Eligible for Study:  13 Years   -   17 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • DSM-IV criteria for schizophrenia; age 13 - 17 years

Exclusion Criteria:

  • Imminent risk of suicide or homicide, as judged by the site investigator; any history of serious or unstable medical illness, including risk for QT prolongation

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00257192


Study chairs or principal investigators

Pfizer CT.gov Call Center,  Study Director,  Pfizer   

More Information

Study ID Numbers:  A1281134
Last Updated:  January 5, 2006
Record first received:  November 21, 2005
ClinicalTrials.gov Identifier:  NCT00257192
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2006-01-10

Resources



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Page Updated: June 1, 2005
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