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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00990626
Other study ID # NIS-NHU-SER-2009/1
Secondary ID
Status Completed
Phase N/A
First received October 1, 2009
Last updated November 16, 2010
Start date October 2009
Est. completion date July 2010

Study information

Verified date November 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Hungary: National Institute of Pharmacy
Study type Observational

Clinical Trial Summary

The purpose of the study is to determine whether the Seroquel XR treatment for 6 months improve the relapse prevention in schizophrenic outpatients


Recruitment information / eligibility

Status Completed
Enrollment 1600
Est. completion date July 2010
Est. primary completion date July 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Schizophrenic outpatients on at least 600 mg Seroquel XR treatment for at least 1 month

Exclusion Criteria:

- Severe cerebro- and cardiovascular disease, severe hepatic impairment, gravidity

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Hungary Research Site Baja
Hungary Research Site Barcs
Hungary Research Site Budapest
Hungary Research Site Cegled
Hungary Research Site Debrecen
Hungary Research Site Dombovar
Hungary Research Site Dunaujvaros
Hungary Research Site Eger
Hungary Research Site Egerszalok
Hungary Research Site Emod
Hungary Research Site Erd
Hungary Research Site Esztergom
Hungary Research Site Godollo
Hungary Research Site Gyongyos
Hungary Research Site Gyor
Hungary Research Site Gyula
Hungary Research Site Heves
Hungary Research Site Hodmezovasarhely
Hungary Research Site Janoshalma
Hungary Research Site Jaszbereny
Hungary Research Site Kalocsa
Hungary Research Site Kecskemet
Hungary Research Site Ketegyhaza
Hungary Research Site Kiskunhalas
Hungary Research Site Kistokaj
Hungary Research Site Miskolc
Hungary Research Site Nagyatad
Hungary Research Site Nagykallo
Hungary Research Site Nagykanizsa
Hungary Research Site Nagykoros
Hungary Research Site Oroshaza
Hungary Research Site Pecs
Hungary Research Site Pomaz
Hungary Research Site Satoraljaujhely
Hungary Research Site Soltvadkert
Hungary Research Site Sopron
Hungary Research Site Sumeg
Hungary Research Site Szeged
Hungary Research Site Szeghalom
Hungary Research Site Szekesfehervar
Hungary Research Site Szekszard
Hungary Research Site Szentes
Hungary Research Site Szigetszentmiklos
Hungary Research Site Szigetvar
Hungary Research Site Szolnok
Hungary Research Site Szombathely
Hungary Research Site Tatabanya
Hungary Research Site Veszprem

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Hungary, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of patients remained relapse free after 6 months of treatment No
Secondary Adherence rate of patients No
Secondary Quality of Life (QoL ) No