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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT00073164

Public ClinicalTrials.gov record NCT00073164. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 1:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study of the Safety and Efficacy of Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone in the Treatment of Schizophrenia

Study identification

NCT ID
NCT00073164
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Abbott
Industry
Enrollment
400 participants

Conditions and interventions

Conditions

Interventions

  • Divalproex Sodium Extended-Release Tablets Drug
  • Olanzapine Drug
  • Risperidone Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2003
Primary completion
Not listed
Completion
Not listed
Last update posted
Aug 3, 2006

Started 2003

United States locations

U.S. sites
35
U.S. states
18
U.S. cities
35
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Tuscaloosa Alabama
Not listed Anaheim California
Not listed Cerritos California
Not listed Chula Vista California
Not listed Garden Grove California
Not listed Glendale California
Not listed Los Angeles California
Not listed San Diego California
Not listed Denver Colorado
Not listed Gainsville Florida
Not listed Melbourne Florida
Not listed North Miami Florida
Not listed Winter Park Florida
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed Hoffman Estates Illinois
Not listed Indianapolis Indiana
Not listed South Bend Indiana
Not listed Shreveport Louisiana
Not listed Rockville Maryland
Not listed Jackson Mississippi
Not listed Clementon New Jersey
Not listed Kenilworth New Jersey
Not listed Holliswood New York
Not listed New York New York
Not listed Butner North Carolina
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Oklahoma City Oklahoma
Not listed Philadelphia Pennsylvania
Not listed Austin Texas
Not listed Irving Texas
Not listed San Antonio Texas
Not listed Falls Church Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00073164, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 3, 2006 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00073164 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →