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Completed Phase 3 Interventional Results available

Conversion To Monotherapy With Lamictal Extended Release Tablets For Treatment Of Partial Epilepsy

ClinicalTrials.gov ID: NCT00355082

Public ClinicalTrials.gov record NCT00355082. 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 23, 2026, 2:07 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, Randomized Conversion to Monotherapy Comparison of Two Doses of Lamotrigine for the Treatment of Partial Seizures

Study identification

NCT ID
NCT00355082
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
226 participants

Conditions and interventions

Interventions

  • lamotrigine, 300 mg/day Drug
  • lamotrigine, 250 mg/day Drug

Drug

Eligibility (public fields only)

Age range
13 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
Apr 30, 2006
Primary completion
Oct 31, 2008
Completion
Oct 31, 2008
Last update posted
Jan 1, 2017

2006 – 2008

United States locations

U.S. sites
67
U.S. states
31
U.S. cities
59
Facility City State ZIP Site status
GSK Investigational Site Alabaster Alabama 35007
GSK Investigational Site Litchfield Park Arizona 85340
GSK Investigational Site Mesa Arizona 85201
GSK Investigational Site Phoenix Arizona 85003
GSK Investigational Site Phoenix Arizona 85013
GSK Investigational Site Tucson Arizona 85724
GSK Investigational Site Tucson Arizona 85741
GSK Investigational Site Fayetteville Arkansas 72703
GSK Investigational Site Los Angeles California 90073
GSK Investigational Site Pasadena California 91105
GSK Investigational Site Santa Ana California 92705
GSK Investigational Site Santa Monica California 90404
GSK Investigational Site Danbury Connecticut 06810
GSK Investigational Site Fairfield Connecticut 06824
GSK Investigational Site Newark Delaware 19713
GSK Investigational Site Jacksonville Florida 32224
GSK Investigational Site Loxahatchee Groves Florida 33470
GSK Investigational Site Sunrise Florida 33351
GSK Investigational Site Tampa Florida 33613
GSK Investigational Site Atlanta Georgia 30338
GSK Investigational Site Atlanta Georgia 30342
GSK Investigational Site Decatur Georgia 30033
GSK Investigational Site Boise Idaho 83702
GSK Investigational Site Chicago Illinois 60611
GSK Investigational Site Chicago Illinois 60637
GSK Investigational Site Flossmoor Illinois 60422
GSK Investigational Site Urbana Illinois 61801
GSK Investigational Site Des Moines Iowa 50309
GSK Investigational Site Lexington Kentucky 40513
GSK Investigational Site Lexington Kentucky 40536
GSK Investigational Site Louisville Kentucky 40202
GSK Investigational Site New Orleans Louisiana 70115
GSK Investigational Site Bethesda Maryland 20817
GSK Investigational Site Glen Burnie Maryland 21061
GSK Investigational Site Pikesville Maryland 21208
GSK Investigational Site Springfield Massachusetts 01104
GSK Investigational Site Detroit Michigan 48202
GSK Investigational Site Minneapolis Minnesota 55455
GSK Investigational Site Saint Cloud Minnesota 56303
GSK Investigational Site Hattiesburg Mississippi 39401
GSK Investigational Site Kansas City Missouri 64111
GSK Investigational Site St Louis Missouri 63104
GSK Investigational Site St Louis Missouri 63110
GSK Investigational Site Henderson Nevada 89014
GSK Investigational Site Las Vegas Nevada 81902
GSK Investigational Site Las Vegas Nevada 89106
GSK Investigational Site Edison New Jersey 08818
GSK Investigational Site Vorhees New Jersey 08043
GSK Investigational Site Lawrence New York 11559
GSK Investigational Site Plainview New York 11803
GSK Investigational Site Syracuse New York 13210
GSK Investigational Site Asheville North Carolina 28803
GSK Investigational Site Columbus Ohio 43210-1296
GSK Investigational Site Oklahoma City Oklahoma 73112
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Sellersville Pennsylvania 18960
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Houston Texas 77025
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site San Antonio Texas 78258
GSK Investigational Site Temple Texas 76502
GSK Investigational Site Midvale Utah 84047
GSK Investigational Site Renton Washington 98055
GSK Investigational Site Charleston West Virginia 25301
GSK Investigational Site Morgantown West Virginia 26506
GSK Investigational Site Madison Wisconsin 53715
GSK Investigational Site Milwaukee Wisconsin 53215

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 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00355082, 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 1, 2017 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00355082 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →