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Predicting efficacy of neuromodulation in epilepsy

Recruiting
Conditions
Epilepsy
Registration Number
NL-OMON23690
Lead Sponsor
Medisch Spectrum Twente
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
5
Inclusion Criteria

• Adult (>=18 year) patients with medically refractory epilepsy, who are candidates for VNS.
• Known with a focal epilepsy with a temporal/frontotemporal seizure-onset zone (as corroborated by EEG or magnetic resonance imaging [MRI]) or a generalized epilepsy.
• A self-reported seizure frequency of at least one seizure per month.

Exclusion Criteria

• Prior brain surgery.
• Cognitive impairments that causes the patient to be unable to onderstand the research purpose and give informed consent.
• Exclusion criteria (for safety issues) to ondergo an MRI scan.
• Planned or expected MRI scan during the period where the subcutaneous electrode is implanted.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
• The primary goal of the pilot study is to test the feasibility and patients' satisfaction of the subcutaneous electrode.<br>• If successful, the study will be expanded to a larger cohort. The primary objective of this larger study is to predict success of VNS in patients with epilepsy using pre-operative features from ultra long-term EEG recordings, resting-state 64-channel EEG and MRI. We will initially aim to predict responders (>50% seizure reduction); this binarized response will be complemented by assessing the likelihood of seizure reduction on a continuous scale.
Secondary Outcome Measures
NameTimeMethod
• To evaluate the correspondence between seizures reported by the patients (using diaries) and the seizures recorded by the subcutaneous electrode.<br>• To study differences in network characteristics derived from 64-channel EEG, and MRI before and after VNS.<br>• To evaluate the effect of VNS on psychologica) well-being including quality of life, anxiety and depression.<br>• To evaluate the effect of VNS on sleep quality (total sleep duration, time to first REM, total time in deep sleep measured with the subcutaneous EEG recording).
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