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Neuronal Excitability of HCN1 Channel Mutations in Dravet Syndrome

NCT02896608 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 92

Last updated 2023-02-15

No results posted yet for this study

Summary

This study addresses the changes in the axonal excitability parameters. It will compare these changes in patients with early infantile epileptic encephalopathy with HCN1 channel mutation and in control patients, with and without epilepsy.

Conditions

Interventions

DEVICE

measure of neuronal excitability

Sponsors & Collaborators

  • Fondation Ophtalmologique Adolphe de Rothschild

    lead NETWORK

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-10-29
Primary Completion
2019-10-16
Completion
2019-10-16

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02896608 on ClinicalTrials.gov