Neuronal Excitability of HCN1 Channel Mutations in Dravet Syndrome
NCT ID: NCT02896608
Last Updated: 2023-02-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
92 participants
OBSERVATIONAL
2015-10-29
2019-10-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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Dravet syndrome - HCN1 channel mutation
early infantile epileptic encephalopathy with HCN1 channel mutation
measure of neuronal excitability
control with epilepsy
measure of neuronal excitability
control without epilepsy
measure of neuronal excitability
Interventions
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measure of neuronal excitability
Eligibility Criteria
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Inclusion Criteria
* control patients with no neurologic pathology (age, gender and body temperature matched)
* epileptic patients (age, gender and body temperature matched)
Exclusion Criteria
15 Years
ALL
Yes
Sponsors
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Fondation Ophtalmologique Adolphe de Rothschild
NETWORK
Responsible Party
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Locations
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Fondation Ophtalmologique Adolphe de Rothschild
Paris, , France
Countries
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Other Identifiers
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AGN_2015_11
Identifier Type: -
Identifier Source: org_study_id
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