An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treatment of Mania/Bipolar Disorder in Children and Adolescents
Public ClinicalTrials.gov record NCT00067262. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Double-Blind, Placebo-Controlled Trial to Evaluate the Safety and Efficacy of Depakote ER for the Treatment of Bipolar Disorder in Children and Adolescents
Study identification
- NCT ID
- NCT00067262
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- Abbott
- Industry
- Enrollment
- 150 participants
Conditions and interventions
Conditions
Interventions
- Divalproex Sodium Extended-Release Tablets Drug
Drug
Eligibility (public fields only)
- Age range
- 10 Years to 17 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
- Feb 28, 2003
- Primary completion
- Not listed
- Completion
- Not listed
- Last update posted
- Aug 3, 2006
Started 2003
United States locations
- U.S. sites
- 16
- U.S. states
- 12
- U.S. cities
- 16
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Stanford University | Stanford | California | 94304 | — |
| Childrens National Medical Center | Washington D.C. | District of Columbia | 20010 | — |
| Not listed | Altamonte Springs | Florida | 32701 | — |
| Professional Clinical Research, Inc. | Miami | Florida | 33161 | — |
| Segal Institute for Clinical Research | North Miami | Florida | 33161 | — |
| Mountain West Clinical Trials | Boise | Idaho | 83704 | — |
| Capstone Clinical Research | Libertyville | Illinois | 60031 | — |
| Cientifica Inc at Praire View, Inc. | Newton | Kansas | 67114 | — |
| Not listed | Lexington | Kentucky | 40509 | — |
| LSU - Health Science Center | New Orleans | Louisiana | 70112 | — |
| Brentwood Research Institute | Shreveport | Louisiana | 71101 | — |
| New Oakland Child/Adoles and Family Center | Clinton Township | Michigan | — | — |
| Mercy Health Research | Chesterfield | Missouri | 63017 | — |
| Cutting Edge Research Group | Oklahoma City | Oklahoma | — | — |
| University of Texas Medical Branch | Galveston | Texas | 77705 | — |
| University of Texas Medical Branch | Houston | Texas | 77058 | — |
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 NCT00067262, 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 22, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00067262 live on ClinicalTrials.gov.