Human Epilepsy Genetics--Neuronal Migration Disorders Study

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
Harvard University Faculty of Medicine
Study ID
NCT00041600
Status
Recruiting
Apply to this trial

Conditions

  • Brain Malformation
  • Cognition Disorder
  • Epilepsy
  • Neuronal Migration Disorder

Eligibility Criteria

Sex
ALL
Age
N/A - N/A
Healthy Volunteers
Not accepted

Study Details

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

Key Dates

Start date
Apr 30, 1996
Status verified
Sep 2023
Primary completion
Jun 30, 2030
Completion
Jun 30, 2030

Study Design

Enrollment
3,500 participants (estimated)

Primary Outcome Measure

Identification and characterization of genes important in normal brain development and associated with brain malformations. [ Time Frame: Ongoing ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Boston Children's Hospital, Walsh LaboratoryBostonMassachusetts02115
Jennifer Neil, MS
[email protected]
617-919-2865
Abbe Lai, MS
617-919-4371
Christopher A. Walsh, M.D., Ph.D. (PRINCIPAL_INVESTIGATOR)

Find similar trials in Boston, MA

By condition
Epilepsy
By specialty
NeurologyBrain disorders
By research site
Boston Children's Hospital, Walsh Laboratory· Boston, MA

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