Seroquel (Quetiapine Fumarate) InPractice Evaluation Programme

NCT ID: NCT00921362

Last Updated: 2009-06-16

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

Total Enrollment

1387 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-05-31

Study Completion Date

2007-01-31

Brief Summary

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Patients eligible for entry into the study have a diagnosis of schizophrenia defined by Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (DSM-IV) criteria and of a chronic or sub-chronic nature.The primary purpose of the study is to observe symptoms changes over 6 months in schizophrenia in patients treated with Seroquel; additionally disease severity and treatment compliance are followed

Detailed Description

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Conditions

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Schizophrenia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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1

Schizophrenia patients under Seroquel treatment

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* To assess at baseline and after treatment administration the severity of the illness in patients with schizophrenia, using the scores obtained after the application of the CGI scale
* To assess the changes in symptoms of patients treated with Seroquel for 24 weeks, using BPRS (Brief Psychiatry Rating Scale) as measuring tool

Exclusion Criteria

* All the patients who have a known hypersensitivity to Seroquel /quetiapine or any of its excipients will not be included in this study.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Principal Investigators

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stina Pentiuc, Med Director

Role: STUDY_DIRECTOR

AstraZeneca Romania

Other Identifiers

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SER-01-S-06

Identifier Type: -

Identifier Source: secondary_id

NIS-NRO-SER-2006/2

Identifier Type: -

Identifier Source: org_study_id

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