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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 Oct 31, 2026, 6:51 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
Aug 2007 (Type not available)
Primary completion
Jul 2010 (Actual)
Completion
Jul 2010 (Actual)
Last update posted
Jan 18, 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 18, 2017 · Synced Oct 31, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00516139 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →