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Priming the Epileptic Brain: tVNS to Improve Efficacy of add-on AED in Patients With Focal Epilepsy (PREP)

17 december 2021 uppdaterad av: Eindhoven University of Technology

Priming the Epileptic Brain - Determining the Effect of Temporarily Addition of Transcutaneous Vagal Nerve Stimulation When Starting an add-on AED (in This Case Brivaracetam) in Patients With Refractory Focal Epilepsy

The most prevalent neurological disorder with also immense burden of disease, epilepsy, is in over 30 percent of patients difficult to treat. The ideal treatment regime would give complete control of disease in an early stage, not only for patient well-being, but also to prevent the onset of persistent pathologic epileptic networks in the brain. The first step in treatment is the trial, and error, of multiple anti-epileptic drugs (AEDs), while invasive brain stimulation (BS) techniques with network modulating properties are saved as a last resort. The investigators hypothesize that pharmacotherapeutic treatment of epilepsy can be more successful after "priming" (preparing) the brain using BS as a short-term neuromodulation treatment. The limitation of testing this hypothesis is the invasive aspect of the most used classic vagal nerve stimulation (VNS) treatment for epilepsy, but the recent development of transcutaneous vagal nerve stimulation (tVNS) offered a possibility to combine chemical and electrical modulation in an earlier stage of disease, which is not tested before. The investigators want to determine the priming effect on the epileptic brain of tVNS, to make it more susceptible to add-on treatment with Brivaracetam (BRV), an AED. In addition, the investigators aim to visualize these changes in the brain because of priming, possibly altered network-organisation.

Studieöversikt

Status

Rekrytering

Betingelser

Intervention / Behandling

Detaljerad beskrivning

Background of the study: The most prevalent neurological disorder with also immense burden of disease, epilepsy, is in over 30 percent of patients difficult to treat. The ideal treatment regime would give complete control of disease in an early stage, not only for patient well-being, but also to prevent the onset of persistent pathologic epileptic networks in the brain. The first step in treatment is the trial, and error, of multiple anti-epileptic drugs (AEDs), while invasive brain stimulation (BS) techniques with network modulating properties are saved as a last resort. The investigators hypothesize that pharmacotherapeutic treatment of epilepsy can be more successful after "priming" (preparing) the brain using BS as a short-term neuromodulation treatment. The limitation of testing this hypothesis is the invasive aspect of the most used classic vagal nerve stimulation (VNS) treatment for epilepsy, but the recent development of transcutaneous vagal nerve stimulation (tVNS) offered a possibility to combine chemical and electrical modulation in an earlier stage of disease, which is not tested before.

Objective of the study: Determine the priming effect on the epileptic brain of tVNS, to make it more susceptible to add-on treatment with Brivaracetam (BRV), an AED. In addition, the investigators aim to visualize these changes in the brain because of priming, possibly altered network-organisation.

Study design: Randomized Controlled Trial. Study population: Adults with a refractory (continuing of seizures despite 2 tried AEDs) focal epilepsy and therefore have an indication for start of Brivaracetam. Intervention (if applicable): One group receives transcutaneous vagal nerve stimulation (tVNS) 4 hours daily for the first 3 months of brivaracetam treatment. Primary study parameters/outcome of the study: Scoring on a composite index combining seizure reduction, improvement of cognition and quality of life. Secondary study parameters/outcome of the study (if applicable): Seizure reduction, seizure freedom rates, seizure severity, cognition, mood state, adverse events tVNS and brivaracetam, change in brain network properties.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness (if applicable): Besides minor temporary side effects no risk is attributed to tVNS. Because of the study one extra visit is necessary, besides regular clinical follow-up. The 3 visits do require some more time than usual because of the questionnaires, MRI and short cognitive tests. The burden of the telephone calls is very limited, since it only consists of a few short questions. Patients with claustrophobia are excluded, but the requirement of lying still can be somewhat uncomfortable. The eye tracking device uses a camera in the video screen, with no burden at all.

Studietyp

Interventionell

Inskrivning (Förväntat)

66

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

  • Namn: Angelique A Stuurman, Msc
  • Telefonnummer: 0031402279777
  • E-post: prep@tue.nl

Studera Kontakt Backup

  • Namn: Rob R Mestrom, Dr
  • Telefonnummer: 0031402279777
  • E-post: prep@tue.nl

Studieorter

    • Noord Brabant
      • Heeze, Noord Brabant, Nederländerna, 5590 AB
        • Rekrytering
        • Stichting Kempenhaeghe
        • Kontakt:
          • Angelique Stuurman
          • Telefonnummer: 0031 0402279777
          • E-post: prep@tue.nl

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Focal epilepsy which is refractory (at least 2 different AEDs tried) and therefore has an indication for start of brivaracetam
  • Age ≥ 18 years.
  • IQ > 70 defined as any form of secondary education

Exclusion Criteria:

  • - Inclusion not possible within 2 weeks after start of brivaracetam
  • History of a progressive cerebral disorder (neurodegenerative diseases, tumours)
  • History of psychogenic nonepileptic seizures (PNES)
  • Inability to provide informed consent
  • Any contra-indication for brivaracetam
  • Current or recent use (exposed ≤ 90 days)
  • Current or recent use (exposed ≤ 90 days) of levetiracetam
  • Current treatment with neurostimulation
  • Inability of handling the tVNS device personally
  • Subjects that have a current diagnosis of cardiac arrhythmic disease
  • Any contraindication for tVNS: pregnancy, active implants (such as cardiac pacemakers of cochlear implants) or cerebral shunts (e.g. ventriculo-peritoneal shunts with valve)
  • Any contraindication for MRI: metallic foreign body, pacemaker, claustrophobia, pregnancy

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: Brivaracetam + Transcutaneous vagal nerve stimulation
Start of Brivaracetam (treatment as usual), combined with tVNS in the first 3 months of treatment
Cerbomed NEMOS
Inget ingripande: Brivaracetam
Start of Brivaracetam (treatment as usual)

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Epilepsy frequency
Tidsram: 6 months
Seizure reduction (in % at 3 and 6 months in respect to baseline)
6 months
Epilepsy frequency
Tidsram: 6 months
Seizure freedom rates (defined as the percentage of subjects with 100% reduction from baseline seizure frequency)
6 months
Seizure severity
Tidsram: 6 months
Assessed by the National Hospital Seizure Severity Scale - NHS3, comparing scores at 3 and 6 months to baseline). Score range 1-27 (higher score = more severe).
6 months

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Brain networks
Tidsram: 3 months
Detect changes in network properties by comparing fMRI (functional MRI) data at 3 months with baseline (independent component analysis)
3 months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Marian M Majoie, Prof. Dr., ACE Kempenhaeghe

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 augusti 2021

Primärt slutförande (Förväntat)

1 juli 2023

Avslutad studie (Förväntat)

1 juli 2023

Studieregistreringsdatum

Först inskickad

2 juli 2021

Först inskickad som uppfyllde QC-kriterierna

17 december 2021

Första postat (Faktisk)

6 januari 2022

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

6 januari 2022

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

17 december 2021

Senast verifierad

1 december 2021

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • PREP_001

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

produkt tillverkad i och exporterad från U.S.A.

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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