The "New" Place of LEVETIRACETAM in the Management of Status Epilepticus in Children

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-17
SponsorUniversity Hospital, Strasbourg, France

About this trial

Status epilepticus is the leading neurological emergency in children, with mortality 2-7% and significant morbidity (10-20%). It is defined as the occurrence of a crisis lasting more than 5 minutes and requiring the implementation of treatment to stop it and thus limit the immediate and long-term consequences.

The research hypothesis is that LEVETIRACETAM is non-inferior to PHENYTOIN in terms of cessation and absence of recurrence of status epilepticus, with better clinical tolerance in children from 3 months to 17 years old, with or without epileptic disease, with or without a history of status epilepticus

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Minor patient aged 3 months to 17 years

2nd line treatment with LEVETIRACETAM or PHENYTOIN after failure of benzodiazepines

Supported in one of the participating centers during the period from November 1, 2019 to May 31, 2023

Subject or parents who have not expressed, after information, their opposition to the reuse of their data for the purposes of this research.

Disqualifiers

Patient or parents having expressed their opposition to participating in the study.

Trial population

Minor patient aged 3 months to 17 years having 2nd line treatment with LEVETIRACETAM or PHENYTOIN after failure of benzodiazepines

Trial design

Design model

Case-control

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Highlight non-inferiority of LEVETIRACETAM compared to PHENYTOIN

The non-inferiority of LEVETIRCETAM in comparison with PHENYTOIN is based on a composite primary endpoint consisting of the total duration of the seizure, the need for another antiepileptic treatment to resolve the seizure or recurrence within 24 hours. following the start of treatment for a new status epilepticus and the total duration of hospitalization. The need for another antiepileptic drug or recurrence is a binary variable with presence (= yes = 1) or absence (= no = 0). The total duration of the crisis is expressed in minutes, and corresponds to the interval between the identification of the event and the objectification of its cessation. The total duration of hospitalization is expressed in days, and corresponds to the duration between the first day of hospitalization (regardless of the location) and the day of discharge (regardless of the department).

Time frame
Up to 2 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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