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Completed Phase 3 Interventional Results available

Lamotrigine Extended-Release In Elderly Patients With Epilepsy

ClinicalTrials.gov ID: NCT00516139

Public ClinicalTrials.gov record NCT00516139. 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 11, 2026, 2:55 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

Lamotrigine Extended-Release in Elderly Patients With Epilepsy

Brief summary

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

This study is being conducted to determine the safety and tolerability of lamotrigine (LTG) in elderly patients with epilepsy. This study will be carried out using an extended-release formulation of lamotrigine (LTG-XR) that will allow once-a-day dosing.

Study identification

NCT ID
NCT00516139
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
122 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
65 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
Jul 31, 2007
Primary completion
Jun 30, 2010
Completion
Jun 30, 2010
Last update posted
Jan 17, 2017

2007 – 2010

United States locations

U.S. sites
63
U.S. states
28
U.S. cities
57
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294-0021
GSK Investigational Site Gilbert Arizona 85234
GSK Investigational Site Litchfield Park Arizona 85340
GSK Investigational Site Phoenix Arizona 85003
GSK Investigational Site Phoenix Arizona 85013
GSK Investigational Site Fresno California 93710
GSK Investigational Site Fullteron California 92835
GSK Investigational Site Irvine California 92618
GSK Investigational Site Los Angeles California 90073
GSK Investigational Site Pasadena California 91106
GSK Investigational Site Fort Collins Colorado 80524
GSK Investigational Site Newark Delaware 19713
GSK Investigational Site Gainesville Florida 32610
GSK Investigational Site Jacksonville Florida 32224
GSK Investigational Site Jacksonville Florida 32266
GSK Investigational Site Melbourne Florida 32901
GSK Investigational Site Miami Florida 33136
GSK Investigational Site Ponte Vedra Beach Florida 32082
GSK Investigational Site Sarasota Florida 34233
GSK Investigational Site Atlanta Georgia 30309
GSK Investigational Site Atlanta Georgia 30322
GSK Investigational Site Suwanee Georgia 30024
GSK Investigational Site Boise Idaho 83702
GSK Investigational Site Springfield Illinois 62702
GSK Investigational Site Fort Wayne Indiana 46805
GSK Investigational Site Indianapolis Indiana 46256
GSK Investigational Site Wichita Kansas 67214
GSK Investigational Site Louisville Kentucky 40202
GSK Investigational Site Scarborough Maine 4074
GSK Investigational Site Burlington Massachusetts 01805
GSK Investigational Site Hopedale Massachusetts 01747
GSK Investigational Site Traverse City Michigan 49684
GSK Investigational Site Minneapolis Minnesota 55422
GSK Investigational Site Saint Paul Minnesota 55102
GSK Investigational Site Chesterfield Missouri 63017
GSK Investigational Site Kansas City Missouri 64111
GSK Investigational Site Henderson Nevada 89014
GSK Investigational Site Camden New Jersey 08103
GSK Investigational Site Newark New Jersey 07103
GSK Investigational Site Summit New Jersey 07901
GSK Investigational Site Cedarhurst New York 11516
GSK Investigational Site Rochester New York 14642
GSK Investigational Site Schenectady New York 12308
GSK Investigational Site Columbus Ohio 43210
GSK Investigational Site Toledo Ohio 43614
GSK Investigational Site Oklahoma City Oklahoma 73112
GSK Investigational Site Philadelphia Pennsylvania 19102
GSK Investigational Site Philadelphia Pennsylvania 19140
GSK Investigational Site Pittsburgh Pennsylvania 15240
GSK Investigational Site Sellersville Pennsylvania 18960
GSK Investigational Site Columbia Tennessee 38401
GSK Investigational Site Cordova Tennessee 38018
GSK Investigational Site Germantown Tennessee 38139
GSK Investigational Site Nashville Tennessee 37232
GSK Investigational Site Dallas Texas 75214
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Houston Texas 77030
GSK Investigational Site Temple Texas 76508
GSK Investigational Site Richmond Virginia 23298
GSK Investigational Site Bremerton Washington 98310
GSK Investigational Site Madison Wisconsin 53715
GSK Investigational Site Milwaukee Wisconsin 53215
GSK Investigational Site Milwaukee Wisconsin 53226

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 NCT00516139, 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 17, 2017 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00516139 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →