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Completed Phase 3 Interventional

Depression And Bipolar Disorder

ClinicalTrials.gov ID: NCT00274677

Public ClinicalTrials.gov record NCT00274677. 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 Sep 13, 2026, 7:37 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

A Multicenter, Double-Blind, Placebo-Controlled, Fixed-Dose, 8-Week Evaluation of the Efficacy and Safety of Lamotrigine in the Treatment of Depression in Patients With Type II Bipolar Disorder

Brief summary

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

This study is an 8-week evaluation of an investigational drug for treating depression in bipolar patients. Depressed patients will be given either an investigational drug or placebo and receive psychiatric assessments of their depression at weekly visits. Study drug and all study-related visits are provided at no cost to the patient. The patient agrees to meet with study research staff for roughly 11 clinic visits.

Study identification

NCT ID
NCT00274677
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
221 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Oct 31, 2003
Primary completion
Jul 31, 2005
Completion
Jul 31, 2005
Last update posted
Sep 14, 2016

2003 – 2005

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
GSK Investigational Site Burbank California 91506
GSK Investigational Site Loma Linda California 92354
GSK Investigational Site San Diego California 92108
GSK Investigational Site Marietta Georgia 30060
GSK Investigational Site Terre Haute Indiana 47802
GSK Investigational Site Shreveport Louisiana 71101
GSK Investigational Site Saint Charles Missouri 63301
GSK Investigational Site Clementon New Jersey 08021
GSK Investigational Site Princeton New Jersey 08540
GSK Investigational Site New York New York 10021
GSK Investigational Site Pleasantville New York 10570
GSK Investigational Site Charlotte North Carolina 28209
GSK Investigational Site Raleigh North Carolina 27609
GSK Investigational Site Beachwood Ohio 44122
GSK Investigational Site Oklahoma City Oklahoma 73118
GSK Investigational Site Eugene Oregon 97401
GSK Investigational Site Columbia South Carolina 29201
GSK Investigational Site Galveston Texas 77555-0188
GSK Investigational Site Houston Texas 77090

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 NCT00274677, 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 Sep 14, 2016 · Synced Sep 13, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00274677 live on ClinicalTrials.gov.

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