# Longitudinal Study of Phenotypic and Developmental Severity in Patients With Dravet Syndrome With SCN1A Gene Mutation

> **NCT07251673** · — · RECRUITING · sponsor: **Assistance Publique - Hôpitaux de Paris** · enrollment: 50 (estimated)

## Conditions studied

- Dravet Syndrome

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT07251673
- **Lead sponsor:** Assistance Publique - Hôpitaux de Paris
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2025-09-15
- **Primary completion:** 2030-10-01
- **Final completion:** 2030-10-01
- **Target enrollment:** 50 (ESTIMATED)
- **Last updated:** 2026-02-03

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07251673

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07251673, "Longitudinal Study of Phenotypic and Developmental Severity in Patients With Dravet Syndrome With SCN1A Gene Mutation". Retrieved via AI Analytics 2026-09-04 from https://api.ai-analytics.org/clinical/NCT07251673. Licensed CC0.

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