Trials / Completed
CompletedNCT02896608
Neuronal Excitability of HCN1 Channel Mutations in Dravet Syndrome
Neuronal Excitability of Hyperpolarization-activated Cyclic Nucleotide-gated (HCN1) Channel Mutations in Dravet Syndrome
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 92 (actual)
- Sponsor
- Fondation Ophtalmologique Adolphe de Rothschild · Network
- Sex
- All
- Age
- 15 Years
- Healthy volunteers
- Accepted
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
| Type | Name | Description |
|---|---|---|
| DEVICE | measure of neuronal excitability |
Timeline
- Start date
- 2015-10-29
- Primary completion
- 2019-10-16
- Completion
- 2019-10-16
- First posted
- 2016-09-12
- Last updated
- 2023-02-15
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT02896608. Inclusion in this directory is not an endorsement.