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Completed Phase 2 Interventional

A 19-week Cognition Study of Levetiracetam in Children With Partial Onset Seizures

ClinicalTrials.gov ID: NCT00105040

Public ClinicalTrials.gov record NCT00105040. 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 May 8, 2026, 7:52 AM 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 19-week, Randomized, Double-blind, Multicenter, Placebo-controlled Safety Study to Evaluate the Cognitive and Neuropsychological Effects of Levetiracetam 20 - 60 mg/kg/Day, Divided in Twice Daily Dosing, as Adjunctive Treatment in Children 4 - 16 Years Old, Inclusive, With Refractory Partial Onset Seizures

Study identification

NCT ID
NCT00105040
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Pharma
Industry
Enrollment
87 participants

Conditions and interventions

Interventions

  • Levetiracetam Drug
  • Placebo (PB) Other

Drug · Other

Eligibility (public fields only)

Age range
4 Years to 16 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
Aug 31, 2004
Primary completion
Feb 28, 2007
Completion
Feb 28, 2007
Last update posted
Mar 1, 2015

2004 – 2007

United States locations

U.S. sites
38
U.S. states
21
U.S. cities
38
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Phoenix Arizona
Not listed Tucson Arizona
Not listed Little Rock Arkansas
Not listed La Jolla California
Not listed Los Angeles California
Not listed Denver Colorado
Not listed Washington D.C. District of Columbia
Not listed Bradenton Florida
Not listed Gainesville Florida
Not listed Loxahatchee Groves Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Tallahassee Florida
Not listed Tampa Florida
Not listed Atlanta Georgia
Not listed Augusta Georgia
Not listed Chicago Illinois
Not listed Voorhees Township New Jersey
Not listed Buffalo New York
Not listed New York New York
Not listed Rochester New York
Not listed Winston-Salem North Carolina
Not listed Cleveland Ohio
Not listed Hershey Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Charleston South Carolina
Not listed Germantown Tennessee
Not listed Dallas Texas
Not listed Fort Worth Texas
Not listed Galveston Texas
Not listed Houston Texas
Not listed Norfolk Virginia
Not listed Richmond Virginia
Not listed Seattle Washington
Not listed Morgantown West Virginia
Not listed Milwaukee Wisconsin

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00105040, 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 Mar 1, 2015 · Synced May 8, 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 NCT00105040 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →