# EXploring novEl Molecular Determinants of DRAvet Syndrome Phenotype Heterogeneity

> **NCT06371794** · NA · ENROLLING_BY_INVITATION · sponsor: **Fondazione Policlinico Universitario Agostino Gemelli IRCCS** · enrollment: 16 (estimated)

## Conditions studied

- Dravet Syndrome

## Interventions

- **PROCEDURE:** skin punch biopsy

## Key facts

- **NCT ID:** NCT06371794
- **Lead sponsor:** Fondazione Policlinico Universitario Agostino Gemelli IRCCS
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2023-07-06
- **Primary completion:** 2025-04-30
- **Final completion:** 2026-05-31
- **Target enrollment:** 16 (ESTIMATED)
- **Last updated:** 2024-04-17

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06371794

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06371794, "EXploring novEl Molecular Determinants of DRAvet Syndrome Phenotype Heterogeneity". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT06371794. Licensed CC0.

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