NCT Number: NCT00034905
A Comparison of Seroquel vs. Risperidone in Schizophrenia
The purpose of this study is to show equal efficacy of both quetiapine and risperidone in subjects treated with study medication for up to 8 weeks.
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Notify MeKey information
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Birmingham, Alabama, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Male / Female, 18-65 years old
- Schizophrenia (as per DSM IV)
Exclusion criteria
- Concurrent use of psychotropic medication
- Does not fulfill moderately ill on CGI
Treatment and study plan
Sponsors and collaborators
Lead sponsor
AstraZeneca
Industry
Registry information
Important dates
- Study start
- 2001
- Primary completion
- 2002
- Study completion
- 2002
- First posted
- May 3, 2002
- Registry last updated
- Jan 4, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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