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Tolerability, Safety, And Efficacy Of Ziprasidone (80 - 160 Mg/D) Versus Olanzapine (10 - 20 Mg/D), Risperidone (4 - 8 Mg/D) Or Quetiapine (300 - 750 Mg/D) In Pretreated Patients With Schizophrenia, Schizoaffective Disorder Or Schizophreniform Disorders - A 12-Week Open-Label, Multicenter Clinical Trial.
Evaluation of the antipsychotic efficacy and safety of ziprasidone versus olanzapine, risperidone or quetiapine in patients with schizophrenia, schizoaffective and schizophreniform disorders under naturalistic conditions of clinical practice
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Pfizer Investigational Site
Aalborg, Denmark
Pfizer Investigational Site
Arhus C, Denmark
Pfizer Investigational Site
Augustenborg, Denmark
Pfizer Investigational Site
Ballerup Municipality, Denmark
Pfizer Investigational Site
Brovst, Denmark
Pfizer Investigational Site
Copenhagen, Denmark
Pfizer Investigational Site
Dianalund, Denmark
Pfizer Investigational Site
Esbjerg, Denmark
Pfizer Investigational Site
Esbjerg N, Denmark
Pfizer Investigational Site
Glostrup Municipality, Denmark
Start Date
November 1, 2001
Completion Date
September 1, 2004
Last Updated
February 21, 2021
290
Estimated participants
ziprasidone versus olanzapine , risperidone or quetiapine
DRUG
Panss , CGI-C, UKU-SERS-Pa
BEHAVIORAL
Blood tests
PROCEDURE
Lead Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
NCT07455929
NCT07460453
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06740383