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Completed Phase 3 Interventional

Study of Aripiprazole in Patients With Bipolar I Disorder With a Major Depression Episode

ClinicalTrials.gov ID: NCT00080314

Public ClinicalTrials.gov record NCT00080314. 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 Oct 22, 2026, 6:53 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, Double-Blind, Placebo-Controlled Study of Aripiprazole in the Treatment of Patients With Bipolar I Disorder With a Major Depressive Episode

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate flexible doses (5-30mg) of aripiprazole versus placebo in patients with bipolar depression.

Study identification

NCT ID
NCT00080314
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
400 participants

Conditions and interventions

Interventions

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
Jan 2004 (Type not available)
Primary completion
Oct 2006 (Actual)
Completion
Oct 2006 (Actual)
Last update posted
Nov 11, 2013

2004 – 2006

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Local Institution Tuscaloosa Alabama — —
Local Institution Little Rock Arkansas — —
Local Institution San Diego California — —
Local Institution Sherman Oaks California — —
Local Institution Norwich Connecticut — —
Local Institution West Haven Connecticut — —
Local Institution Jacksonville Florida — —
Local Institution Maitland Florida — —
Local Institution Orlando Florida — —
Local Insstitution Honolulu Hawaii — —
Local Institution Chicago Illinois — —
Local Institution Lake Charles Louisiana — —
Local Institution Rockville Maryland — —
Local Institution Durham North Carolina — —
Local Institution Raleigh North Carolina — —
Local Institution Beachwood Ohio — —
Local Institution Dayton Ohio — —
Local Institution Oklahoma City Oklahoma — —
Local Institution Portland Oregon — —
Local Institution Media Pennsylvania — —
Local Institution Memphis Tennessee — —
Local Institution Austin Texas — —
Local Institution Dallas Texas — —
Local Institution Houston Texas — —
Local Institution Lake Jackson Texas — —
Local Institution Wichita Falls Texas — —
Local Institution Arlington Virginia — —
Local Institution Bellevue Washington — —

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 NCT00080314, 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 Nov 11, 2013 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00080314 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →