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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 December 2017 |
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Main ID: |
NCT02408627 |
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Date of registration:
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31/03/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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EEG@HOME (Phase 3a of the Project, Comparison of EEG-recordings)
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Scientific title:
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Date of first enrolment:
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January 2015 |
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Target sample size:
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3 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02408627 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized. Intervention model: Crossover Assignment. Primary purpose: Diagnostic. Masking: Single (Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Belgium
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Epilepsy patients with prominent interictal epileptiform discharges (IEDs) on EEG
Exclusion Criteria:
- Epilepsy patients with no prominent interictal epileptiform discharges (IEDs) on EEG
Age minimum:
6 Years
Age maximum:
80 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Epilepsy
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Intervention(s)
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Device: EEG
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Primary Outcome(s)
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EEG signal quality (visual and clinical) (scale)
[Time Frame: 10 minutes]
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User experience (questionnaire)
[Time Frame: 10 minutes]
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EEG signal quality (technical) (signal to noise ratio)
[Time Frame: 10 minutes]
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Secondary ID(s)
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EC/2014/1283
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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