MedPath

In-home EEG monitoring in suspected epilepsy.

Recruiting
Conditions
The routine diagnostics and the new approach, 24-48h in-home EEG monitoring, will be studied in patients evaluated for epilepsy.
Registration Number
NL-OMON28676
Lead Sponsor
M.J.A.M. van Putten MD PhDMedisch Spectrum TwenteAfdeling Klinische Neurofysiologie
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

1. Seeing neurologist for suspected epilepsy after first insult;

2. Age above 18 years;

Exclusion Criteria

Patients who have any experience with the current routine EEG procedure in epilepsy diagnosis will be excluded from participation.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Diagnostic accuracy of the 24-48h in-home EEG monitoring procedure in epilepsy, in terms of senstivitiy and specificity.
Secondary Outcome Measures
NameTimeMethod
1. The number of hospital visits from first visit to diagnosis;<br /><br>2. The time-to-diagnosis;<br /><br>3. Direct and indirect costs related to the diagnostic procedure;<br /><br>4. Usability of the EEG equipment including user experience;<br /><br>5. Accuracy of computer algorithms for analysis of the EEG.
© Copyright 2025. All Rights Reserved by MedPath