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Completed Phase 2 Interventional Results available

A Study Designed to Test the Effectiveness and Safety of Treating Patients With Lacosamide for Migraine Prophylaxis

ClinicalTrials.gov ID: NCT00440518

Public ClinicalTrials.gov record NCT00440518. 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 Jun 26, 2026, 1:27 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, Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of 100mg/Day and 300mg/Day Lacosamide for Migraine Prophylaxis.

Study identification

NCT ID
NCT00440518
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Pharma
Industry
Enrollment
218 participants

Conditions and interventions

Conditions

Interventions

  • Lacosamide Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 65 Years
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
Jan 31, 2007
Primary completion
Jun 30, 2008
Completion
Jun 30, 2008
Last update posted
Jul 16, 2018

2007 – 2008

United States locations

U.S. sites
24
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801
Not listed Little Rock Arkansas 72205
Not listed Walnut Creek California
Not listed Boulder Colorado 80304
Not listed Palm Beach Gardens Florida 33410
Not listed South Miami Florida 33143
Not listed Sunrise Florida 33351
Not listed Conyers Georgia 30094
Not listed Evansville Indiana
Not listed Wellesley Hills Massachusetts 02481
Not listed Worcester Massachusetts 01605
Not listed Ann Arbor Michigan 48104
Not listed Springfield Missouri 65807
Not listed St Louis Missouri 63141
Not listed Albany New York 12205
Not listed Greensboro North Carolina 27401
Not listed Matthews North Carolina 28105
Not listed Cleveland Ohio 44121
Not listed Oklahoma City Oklahoma
Not listed Nashville Tennessee 37203
Not listed Houston Texas 77004
Not listed San Antonio Texas 78258
Not listed Alexandria Virginia
Not listed Seattle Washington 98122

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 NCT00440518, 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 Jul 16, 2018 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00440518 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →