Efficacy and Safety of Quetiapine in Treating Affective Symptoms of Patients With First-episode psychosis-a Pilot Study
NCT00511277 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2011-06-21
Summary
The purpose of this study is:
To investigate whether a treatment with quetiapine for six months in patients with first-episode psychosis may be effective in treating depressive symptoms.
To investigate whether a treatment with quetiapine for six months in patients with first-episode psychosis may be effective in mania-like symptoms and to evaluate the general efficacy in psychopathology as well as the safety and tolerability of quetiapine.
Conditions
Interventions
- DRUG
-
Seroquel®
dosage form: oral, dosage: 300-800mg/d, frequency: twice daily
Sponsors & Collaborators
-
University of Göttingen
collaborator OTHER -
Institut fuer anwendungsorientierte Forschung und klinische Studien GmbH
lead OTHER
Principal Investigators
-
Peter Falkai, MD PhD · Department of Psychiatry and Psychotherapy, GEORG-AUGUST-UNIVERSITY GÖTTINGEN, GERMANY
-
Thomas Wobrock, MD PhD · Department of Psychiatry and Psychotherapy, GEORG-AUGUST-UNIVERSITY GÖTTINGEN, GERMANY
-
Andreas Heinz, MD PhD · Department of Psychiatry and Psychotherapy, Charité Campus Mitte Berlin, Germany
-
Georg Juckel, MD PhD · Department of Psychiatry, Ruhr University Bochum, Germany
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 45 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-08-31
- Primary Completion
- 2010-10-31
- Completion
- 2011-04-30
Countries
- Germany
Study Locations
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