Partial sleep deprivation in long-term video-EEG monitoring

Completed

• Conditions: Seizures; 10039911

• Registration Number: NL-OMON44367
• Lead Sponsor: Stichting Epilepsie Instellingen Nederland

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 200

Inclusion Criteria

People above the age of 18 years with paroxismal neurological events, with a clinical suspicion of (focal) epilepsy.

Exclusion Criteria

Mentally disabled people
Most likely diagnosis of idiopathic generalized epilepsy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The difference in number of participants in which a habitual event occurred<br /><br>during the EMU recording between the two study groups.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- identification of clinical characteristics that are associated with the<br /><br>probability that sleep deprivation can provoke clinical events (etiology of<br /><br>events, specific type of epilepsy/seizures).<br /><br>- The difference between the two intervention groups concerning the time to the<br /><br>recording of the first habitual paroxysmal neurological event and the<br /><br>wake/sleep state and time of the day in which the events occurs.<br /><br>- The difference between the two intervention groups concerning the occurrence<br /><br>of the following adverse events: generalized tonic-clonic seizures, seizure<br /><br>clustering.</p><br>