# Genetic Basis of Idiopathic Focal Epilepsies With Cognitif Deficits

> **NCT00851331** · NA · UNKNOWN · sponsor: **University Hospital, Strasbourg, France**

## Conditions studied

- Epilepsy

## Interventions

- **GENETIC:** genome analyzes (genetic defects and pathophysiological mechanisms )

## Key facts

- **NCT ID:** NCT00851331
- **Lead sponsor:** University Hospital, Strasbourg, France
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** —
- **Primary completion:** —
- **Final completion:** —
- **Target enrollment:** — (—)
- **Last updated:** 2009-02-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00851331

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00851331, "Genetic Basis of Idiopathic Focal Epilepsies With Cognitif Deficits". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT00851331. Licensed CC0.

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