Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone in the Treatment of Schizophrenia

Completed · Phase 2

Conditions studied: Schizophrenia

In brief

The purpose of this study is to assess the 14-day and 12-week safety and efficacy of Depakote ER used in combination with either olanzapine or risperidone versus antipsychotic monotherapy with olanzapine or risperidone for the treatment of schizophrenia.

Key facts

Study ID

NCT00073164

Run by

Abbott

People needed

400

Starts

2003-07-01

Last updated by the study team

2006-08-04

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Study site — Birmingham, Alabama, United States
• Study site — Tuscaloosa, Alabama, United States
• Study site — Anaheim, California, United States
• Study site — Cerritos, California, United States
• Study site — Chula Vista, California, United States
• Study site — Garden Grove, California, United States
• Study site — Glendale, California, United States
• Study site — Los Angeles, California, United States
• Study site — San Diego, California, United States
• Study site — Denver, Colorado, United States
• Study site — Gainsville, Florida, United States
• Study site — Melbourne, Florida, United States
• Study site — North Miami, Florida, United States
• Study site — Winter Park, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Hoffman Estates, Illinois, United States
• Study site — Indianapolis, Indiana, United States
• Study site — South Bend, Indiana, United States
• Study site — Shreveport, Louisiana, United States
• Study site — Rockville, Maryland, United States
• Study site — Jackson, Mississippi, United States
• Study site — Clementon, New Jersey, United States
• Study site — Kenilworth, New Jersey, United States
• Study site — Holliswood, New York, United States

Full record on ClinicalTrials.gov

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