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Completed Phase 3 Interventional Results available

Pediatric Bipolar Depression

ClinicalTrials.gov ID: NCT00811473

Public ClinicalTrials.gov record NCT00811473. 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 22, 2026, 11:04 PM EDT

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

Official title

An 8-week, Multicenter, Double-blind, Randomized, Parallel-group, Placebo-controlled Study of the Efficacy and Safety of Quetiapine Fumarate (SEROQUEL) Extended-Release in Children and Adolescent Subjects With Bipolar Depression

Study identification

NCT ID
NCT00811473
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
193 participants

Conditions and interventions

Interventions

  • Quetiapine XR Drug
  • Placebo 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
Dec 31, 2008
Primary completion
Oct 31, 2010
Completion
Oct 31, 2010
Last update posted
Jul 14, 2014

2009 – 2010

United States locations

U.S. sites
31
U.S. states
24
U.S. cities
31
Facility City State ZIP Site status
Research Site Dothan Alabama
Research Site Scottsdale Arizona
Research Site Little Rock Arkansas
Research Site Escondido California
Research Site Bradenton Florida
Research Site Gainsville Florida
Research Site North Miami Florida
Research Site Tampa Florida
Research Site Atlanta Georgia
Research Site Smyrna Georgia
Research Site Eagle Idaho
Research Site Hoffman Estates Illinois
Research Site Terre Haute Indiana
Research Site Overland Park Kansas
Research Site Wichita Kansas
Research Site Clinton Township Michigan
Research Site Minneapolis Minnesota
Research Site Flowood Mississippi
Research Site St Louis Missouri
Research Site Lincoln Nebraska
Research Site Rochester New York
Research Site Cincinnati Ohio
Research Site Cleveland Ohio
Research Site Mason Ohio
Research Site Oklahoma City Oklahoma
Research Site Charleston South Carolina
Research Site Memphis Tennessee
Research Site Wharton Texas
Research Site Virginia Beach Virginia
Research Site Bothell Washington
Research Site Milwaukee Wisconsin

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00811473, 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 Jul 14, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00811473 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →