CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 226 enrolled
Drug / intervention
lamotrigine, 300 mg/day +1 moredrug
Likely dose
lamotrigine, 300 mg/dayfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00355082
NCT00355082Phase 3Completed

A Multicenter, Double-Blind, Randomized Conversion to Monotherapy Comparison of Two Doses of Lamotrigine for the Treatment of Partial Seizures

GlaxoSmithKline·interventional·Posted Jul 21, 2006·Updated Jan 2, 2017

In Brief

A Phase 3 clinical trial evaluating lamotrigine, 300 mg/day and lamotrigine, 250 mg/day for Epilepsy, Partial. Completed, enrolled 226 participants across 103 sites in 8 countries.

Detailed Summary

This study is being conducted to determine the effectiveness of a lower monotherapy dose of lamotrigine than that currently approved.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Chile, Costa Rica, Puerto Rico, Russia, South Korea, Ukraine, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 21, 2006
Enrollment StartMay 1, 2006
Primary CompletionNov 1, 2008
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 19.9 years ago

Interventions

lamotrigine, 300 mg/daydrug

300 mg/day

lamotrigine, 250 mg/daydrug

250 mg/day