ClinicalTrials.gov record
Completed Phase 3 Interventional

Efficacy and Safety of Quetiapine Fumarate (SEROQUEL®) in the Treatment of Alcohol Dependency in Patients With Bipolar Disorder

ClinicalTrials.gov ID: NCT00114686

Public ClinicalTrials.gov record NCT00114686. 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 May 8, 2026, 2:56 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 Multicenter, Randomized, Placebo-Controlled, Parallel-Group, Double-Blind, Phase III Study to Compare the Efficacy and Safety of Quetiapine Fumarate (SEROQUEL®) Versus Placebo as Adjunct Therapy With Mood Stabilizers (Lithium or Divalproex) for the Treatment of Alcohol Dependence in Patients With Bipolar I Disorder

Study identification

NCT ID
NCT00114686
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
350 participants

Conditions and interventions

Interventions

  • Quetiapine fumarate Drug
  • divalproex Drug
  • lithium Drug

Drug

Eligibility (public fields only)

Age range
21 Years to 60 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, 2005
Primary completion
Not listed
Completion
Mar 31, 2007
Last update posted
Jan 3, 2013

2006 – 2007

United States locations

U.S. sites
38
U.S. states
21
U.S. cities
38
Facility City State ZIP Site status
Research Site Cerritos California
Research Site San Diego California
Research Site New Haven Connecticut
Research Site Jacksonville Florida
Research Site Maitland Florida
Research Site Orlando Florida
Research Site Eagle Idaho
Research Site Shreveport Louisiana
Research Site Glen Burnie Maryland
Research Site Boston Massachusetts
Research Site St Louis Missouri
Research Site Moorestown New Jersey
Research Site Albuquerque New Mexico
Research Site New York New York
Research Site Staten Island New York
Research Site The Bronx New York
Research Site Chapel Hill North Carolina
Research Site Research Triangle Park North Carolina
Research Site Cincinnati Ohio
Research Site Cleveland Ohio
Research Site Dayton Ohio
Research Site Portland Oregon
Research Site Media Pennsylvania
Research Site Philadelphia Pennsylvania
Research Site Pittsburgh Pennsylvania
Research Site Columbia South Carolina
Research Site Memphis Tennessee
Research Site Nashville Tennessee
Research Site Austin Texas
Research Site Dallas Texas
Research Site Houston Texas
Research Site San Antonio Texas
Research Site Wichita Falls Texas
Research Site Richmond Virginia
Research Site Bellevue Washington
Research Site Kirkland Washington
Research Site Seattle 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00114686, 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 Jan 3, 2013 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00114686 live on ClinicalTrials.gov.

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