Clinical trial
Human Epilepsy Genetics--Neuronal Migration Disorders Study
NCT00041600 · Harvard University Faculty of Medicine, Other · Recruiting
Key facts
| NCT number | NCT00041600 |
|---|---|
| Title | Human Epilepsy Genetics--Neuronal Migration Disorders Study |
| Official title | Human Epilepsy Genetics--Neuronal Migration Disorders Study |
| Lead sponsor | Harvard University Faculty of Medicine, Other |
| Collaborators | National Institute of Neurological Disorders and Stroke (NINDS) NIH Howard Hughes Medical Institute |
| Status | Recruiting |
| Study type | Observational |
| Conditions | Brain Malformation, Neuronal Migration Disorder, Cognition Disorder, Epilepsy |
| Enrollment | 3,500 |
| Start date | Apr 1, 1996 |
| Primary completion | Jun 1, 2030 |
| Completion | Jun 1, 2030 |
| First posted | Jul 12, 2002 |
| Last update posted | Sep 21, 2023 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- 1–9 FDA inspections linked to this trial
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: