Multicentre Real-life Follow-up Study of Rare Epileptic Syndromes in Children and Adolescents

Last updated: February 23, 2026
Sponsor: Assistance Publique - Hôpitaux de Paris
Overall Status: Active - Recruiting

Phase

N/A

Condition

Seizure Disorders (Pediatric)

Unverricht-lundborg Syndrome

Epilepsy

Treatment

N/A

Clinical Study ID

NCT05126914
P210776
  • Ages < 15
  • All Genders

Study Summary

Rare epilepsies as a whole account for 20-30% of epilepsies, but knowledge about prognostic factors is currently limited. This means that it is difficult to provide adequate information to families at diagnosis and during follow-up. Prognostic factors are also important for management as they can have an impact on the patient's outcome (time to intervention, choice of one molecule over another, etc.). Finally, few treatments are currently available for these epilepsies. One of the limitations to the development of treatments is the lack of real life data as it is difficult to create reliable primary endpoints such as the rate of patients becoming seizure free naturally compared to a therapeutic intervention.

The aim of this real-life study is to evaluate the response to treatment as well as to see the evolution of cognitive and psychiatric comorbidities. As explained above, there are very few randomised trials except for 3 rare epilepsies (infantile spasm syndrome, Dravet syndrome, Lennox-Gastaut syndrome). This has led to the virtual absence of management recommendations, including for the three syndromes mentioned above, where attempts at treatment algorithms have been proposed, although these have not been able to be considered as evidence-based recommendations.

As a result, there is some diversity in the management of rare epilepsies from one centre to another. However, this diversity in management can be an asset in a real-life study. This will make it possible to compare different management methods, both in terms of seizure control and medium-term outcome.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Diagnosis for rare epilepsy (based on ORPHA codes)

  • holders of parental authority not opposed

  • Be followed in one of the declared centers of the study

Exclusion

Exclusion Criteria:

  • opposition from the holders of parental authority or the patient

Study Design

Total Participants: 1000
Study Start date:
December 11, 2025
Estimated Completion Date:
December 31, 2028

Connect with a study center

  • CHU Angers

    Angers 3037656, 49933
    France

    Active - Recruiting

  • CHU de Bordeaux

    Bordeaux 3031582, 33076
    France

    Active - Recruiting

  • CHU de Brest - Hôpital de la Cavale Blanche

    Brest 3030300, 29200
    France

    Active - Recruiting

  • CHRU Lille

    Lille 2998324, 59000
    France

    Active - Recruiting

  • HFME - HospiceS Civils De Lyon

    Lyon 2996944, 69000
    France

    Active - Recruiting

  • Hôpital La Timone - APHM

    Marseille 2995469, 13005
    France

    Active - Recruiting

  • Hopital Robert Debré - Neurologie

    Paris, 75019
    France

    Site Not Available

  • Hopital Robert Debré - Neurologie

    Paris 2988507, 75019
    France

    Active - Recruiting

  • Hôpital Necker - APHP

    Paris 2988507, 75015
    France

    Active - Recruiting

  • CHU Strasbourg- Hôpital de Hautepierre

    Strasbourg 2973783, 67098
    France

    Active - Recruiting

  • Hôpital Purpan - CHU de Toulouse

    Toulouse 2972315, 31000
    France

    Active - Recruiting

  • CHU de Tours - hôpital Clocheville

    Tours 2972191, 37044
    France

    Active - Recruiting

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.