# Evaluation of the Diagnostic Contribution of High-throughput Exome Sequencing for Patients With Convulsive Encephalopathy of Unknown Etiology: Pilot Study to Improve Genetic Counselling

> **NCT03652246** · — · COMPLETED · sponsor: **Centre Hospitalier Universitaire Dijon** · enrollment: 15 (actual)

## Conditions studied

- Epileptic Encephalopathy of Unindentified Genetic Origin

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT03652246
- **Lead sponsor:** Centre Hospitalier Universitaire Dijon
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2013-09
- **Primary completion:** 2014-09
- **Final completion:** 2014-12
- **Target enrollment:** 15 (ACTUAL)
- **Last updated:** 2026-03-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03652246

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03652246, "Evaluation of the Diagnostic Contribution of High-throughput Exome Sequencing for Patients With Convulsive Encephalopathy of Unknown Etiology: Pilot Study to Improve Genetic Counselling". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT03652246. Licensed CC0.

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