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Completed No phase listed Observational

Developmental Effects On Children Of Women Who Take Antiepileptic Drugs During Pregnancy

ClinicalTrials.gov ID: NCT00021866

Public ClinicalTrials.gov record NCT00021866. 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 1, 2026, 11:04 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

Neurodevelopmental Effects of Antiepileptic Drugs II: the NEAD Study

Brief summary

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

The purpose of this study is to determine if antiepileptic drugs (AEDs) differ in their neurodevelopmental effects. Specifically, do the children of the women with epilepsy differ in their behavioral and cognitive development depending on which AED their mother takes during pregnancy?

Study identification

NCT ID
NCT00021866
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Emory University
Other
Enrollment
331 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
Sex
Female
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, 2000
Primary completion
Jul 31, 2010
Completion
Jul 31, 2012
Last update posted
Nov 10, 2013

2000 – 2012

United States locations

U.S. sites
20
U.S. states
17
U.S. cities
20
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 32294
Arizona Health Sciences Tucson Arizona 85724
University of Southern California Los Angeles California 90033
Georgetown University Washington D.C. District of Columbia 20007
Emory University Atlanta Georgia 30322
Medical College of Georgia Augusta Georgia 30912
RUSH University Medical Center Chicago Illinois 60612
Via Christi Medical Center Wichita Kansas 67214
Brigham & Womens' Hospital Boston Massachusetts 02115
Henry Ford Hospital Detroit Michigan 48202
Minnesota Epilepsy Group Saint Paul Minnesota 55102
Columbia University New York New York 10032
Wake Forest University Baptist Medical Center Winston-Salem North Carolina 27157
University of Cincinnati Cincinnati Ohio 45219
Case Western Reserve University Cleveland Ohio 44102
Ohio State University Columbus Ohio 43210
Riddle Health Care II Media Pennsylvania 19063
Baylor Medical Center Irving Texas 75061
University of Utah Salt Lake City Utah 84132
University of Washington Seattle Washington 98104

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00021866, 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 Nov 10, 2013 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00021866 live on ClinicalTrials.gov.

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