# Clinical Interest of a Genetic Diagnosis in Early Infant Epilepsy, Paraclinical and Therapeutic Management, and Psychological Impact of Families

> **NCT05455333** · — · UNKNOWN · sponsor: **University Hospital, Strasbourg, France** · enrollment: 75 (estimated)

## Conditions studied

- Early Infant Epilepsy

## Interventions

- **OTHER:** Questionnaires

## Key facts

- **NCT ID:** NCT05455333
- **Lead sponsor:** University Hospital, Strasbourg, France
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2022-08
- **Primary completion:** 2022-08
- **Final completion:** 2022-12
- **Target enrollment:** 75 (ESTIMATED)
- **Last updated:** 2022-08-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05455333

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05455333, "Clinical Interest of a Genetic Diagnosis in Early Infant Epilepsy, Paraclinical and Therapeutic Management, and Psychological Impact of Families". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT05455333. Licensed CC0.

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