Clinical trial

Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug…

NCT00306475 · Northwestern University, Other · Completed

Key facts

NCT number NCT00306475
Title Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (APD) Improve Cognition And Psychopathology In Outpatients With Schizophrenia (SCH) Or Schizoaffective Disorder (SAD)?
Official title Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (APD) Improve Cognition And Psychopathology In Outpatients With Schizophrenia (SCH) Or Schizoaffective Disorder (SAD)?
Lead sponsor Northwestern University, Other
Collaborators National Alliance for Research on Schizophrenia and Depression Abbott Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Schizophrenia, Schizoaffective Disorder
Intervention type Drug
Interventions Divalproex Sodium Extended-Release Tablets, placebo
Enrollment 60
Start date Mar 1, 2006
Primary completion Apr 1, 2008
Completion Apr 1, 2008
First posted Mar 23, 2006
Last update posted Jun 27, 2025
Countries United States

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies