A Comparison of Seroquel vs. Risperidone in Schizophrenia

NCT ID: NCT00034905

Last Updated: 2013-01-04

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

Clinical Phase

PHASE4

Study Classification

INTERVENTIONAL

Study Start Date

2001-07-31

Study Completion Date

2002-09-30

Brief Summary

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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.

Detailed Description

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Conditions

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Schizophrenia

Study Design

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Primary Study Purpose

TREATMENT

Interventions

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quetiapine fumarate vs risperidone

Intervention Type DRUG

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Locations

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Birmingham, Alabama, United States

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Phoenix, Arizona, United States

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Anaheim, California, United States

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Cerritos, California, United States

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Chula Vista, California, United States

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Glendale, California, United States

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Hawthorne, California, United States

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Long Beach, California, United States

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San Diego, California, United States

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Santa Ana, California, United States

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Torrance, California, United States

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Farmington, Connecticut, United States

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New Haven, Connecticut, United States

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Washington D.C., District of Columbia, United States

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Miami, Florida, United States

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Miami Beach, Florida, United States

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North Miami, Florida, United States

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Winter Park, Florida, United States

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Atlanta, Georgia, United States

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Hoffman Estates, Illinois, United States

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Prairie Village, Kansas, United States

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Wichita, Kansas, United States

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New Orleans, Louisiana, United States

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Shreveport, Louisiana, United States

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Baltimore, Maryland, United States

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Boston, Massachusetts, United States

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Worcester, Massachusetts, United States

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Ann Arbor, Michigan, United States

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New Baltimore, Michigan, United States

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Kansas City, Missouri, United States

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St Louis, Missouri, United States

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Reno, Nevada, United States

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Clementon, New Jersey, United States

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Lyons, New Jersey, United States

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Summit, New Jersey, United States

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Albuquerque, New Mexico, United States

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Holliswood, New York, United States

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Montrose, New York, United States

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New York, New York, United States

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Oceanside, New York, United States

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The Bronx, New York, United States

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White Plains, New York, United States

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Butner, North Carolina, United States

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Beachwood, Ohio, United States

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Chagrin Falls, Ohio, United States

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Cincinnati, Ohio, United States

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Columbus, Ohio, United States

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Oklahoma City, Oklahoma, United States

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Media, Pennsylvania, United States

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Pittsburgh, Pennsylvania, United States

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Memphis, Tennessee, United States

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Nashville, Tennessee, United States

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Austin, Texas, United States

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Houston, Texas, United States

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Terrell, Texas, United States

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Waco, Texas, United States

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Salt Lake City, Utah, United States

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Falls Church, Virginia, United States

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Richmond, Virginia, United States

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Virginia Beach, Virginia, United States

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Kirkland, Washington, United States

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Tacoma, Washington, United States

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Vancouver, Washington, United States

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West Allis, Wisconsin, United States

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Countries

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United States

Other Identifiers

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5077US/0043

Identifier Type: -

Identifier Source: org_study_id

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