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COMPLETED

Study of Antiepileptic Drug Effects on Child Development

NCT00353886 · View on ClinicalTrials.gov ↗

Study Summary

The specific aim of this study is to determine if in utero exposure produces differential antiepileptic drug (AED) effects on subsequent cognitive abilities and behavioral abnormalities in children

Conditions Studied

Interventions

  • PROCEDURE TONI-3
  • PROCEDURE WRAT-3
  • PROCEDURE Connor's Rating Scales PRS & TRS
  • PROCEDURE Peabody Picture Vocabulary Test
  • PROCEDURE Children's Memory Scale

Study Locations (10)

Georgia

  • Emory University School of Medicine — Atlanta
  • Medical College of Georgia — Augusta

California

  • University of Southern California — Los Angeles

District of Columbia

  • Georgetown University — Washington D.C.

Florida

  • University of Florida — Gainesville

Massachusetts

  • Boston University — Boston

Michigan

  • Henry Ford Hospital — Detroit

Minnesota

  • Minnesota Epilepsy Group — Saint Paul

Ohio

  • Case Western Reserve University — Cleveland

Trial Details

FieldValue
Enrollment Target 81 participants
Start Date 2002-09
Est. Completion 2007-06

Sponsor

Augusta University

126 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00353886

The ClinicalTrials.gov registry entry for NCT00353886 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 81 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Augusta University, which has 126 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Epilepsy appearing as the primary indexed condition, and to 5 interventions — of which TONI-3 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00353886 reports 10 study locations spanning 9 distinct geographic areas — top geographies include Georgia, California, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00353886 about?

NCT00353886 is a clinical study titled "Study of Antiepileptic Drug Effects on Child Development". The specific aim of this study is to determine if in utero exposure produces differential antiepileptic drug (AED) effects on subsequent cognitive abilities and behavioral abnormalities in children

What is the current status of trial NCT00353886?

This trial is currently completed. The enrollment target is 81 participants. The study started on 2002-09. Estimated completion is 2007-06.

What conditions does trial NCT00353886 study?

This clinical trial studies the following conditions: Epilepsy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00353886?

The interventions under investigation include: TONI-3 (PROCEDURE), WRAT-3 (PROCEDURE), Connor's Rating Scales PRS & TRS (PROCEDURE), Peabody Picture Vocabulary Test (PROCEDURE), Children's Memory Scale (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00353886?

This trial is sponsored by Augusta University, which has 126 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00353886 being conducted?

This trial has 10 study locations across California, District of Columbia, Florida, Georgia, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial