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NCT00041600 · ClinicalTrials.gov registry record

Human Epilepsy Genetics--Neuronal Migration Disorders Study

A clinical trial of Epilepsy and Cognition Disorder, sponsored by Harvard University Faculty of Medicine.

Recruiting
Registry status
3,500
Enrollment target
1
Study location

NCT00041600: Recruiting study of Epilepsy and Cognition Disorder, sponsored by Harvard University Faculty of Medicine.

NCT00041600 is a study of Epilepsy and Cognition Disorder that is actively recruiting participants, run by Harvard University Faculty of Medicine. The registered enrollment target is 3,500 participants, above the 931-participant average among 160 other Epilepsy trials with a reported enrollment target (276% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00041600, a study of Epilepsy and Cognition Disorder, is actively recruiting participants, sponsored by Harvard University Faculty of Medicine.

RECRUITING
Registry status
3,500 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.

Primary Outcome

Genetic variants associated with disorder of brain development

Study Locations (1)

Massachusetts

  • Boston Children's Hospital, Walsh Laboratory - Boston

Trial Details

FieldValue
Enrollment Target 3,500 participants
Start Date 1996-04
Est. Completion 2030-06

What NCT00041600 shows while recruiting

NCT00041600 is an observational study that tracks outcomes without assigning an intervention. Its 3,500 participants enrollment target places it among the larger protocols in the corpus, above the 931-participant average among 160 other Epilepsy trials with a reported enrollment target (276% higher).

The record links to 4 conditions, with Epilepsy appearing as the primary indexed condition, and to 0 interventions.

NCT00041600 reports a single indexed study location in Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00041600 about?

NCT00041600 is a clinical study titled "Human Epilepsy Genetics--Neuronal Migration Disorders Study". The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.

What is the current status of trial NCT00041600?

This trial is currently recruiting. The enrollment target is 3,500 participants. The study started on 1996-04. Estimated completion is 2030-06.

What conditions does trial NCT00041600 study?

This clinical trial studies the following conditions: Epilepsy, Cognition Disorder, Brain Malformation, Neuronal Migration Disorder.

Who is sponsoring clinical trial NCT00041600?

This trial is sponsored by Harvard University Faculty of Medicine, which has 9 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00041600 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Epilepsy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00041600's enrollment target sits among peer trials

3,500 5th of 160 higher than 156 of 160 other Epilepsy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Epilepsy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00041600, the US trial registry maintained by the National Library of Medicine. NCT00041600 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.