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Study identifier: NCT06549426 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Treatment of ELectroencephalographic STatus Epilepticus After Cardiopulmonary Resuscitation-2 (TELSTAR-2)

Condition: Coma · Electrographic Status Epilepticus  ·  Sponsor: University of Twente

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this comparative effectiveness trial is to study electrographic status epilepticus (ESE) treatment in comatose patients after cardiac arrest. The main questions the trial aims to answer are: * Does ESE treatment improve outcome? * What is the impact of ESE treatment on healthcare costs? Participants in the the intervention group will receive standard care completed with anti-seizure treatment. The control group will receive standard care without anti-seizure treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Jeannette Hofmeijer, MD  ·  +31 53 489 4835  ·  j.hofmeijer@utwente.nl

Nicolas Gaspard, MD  ·  +32 2 555 46 22  ·  nicolas.gaspard@hubruxelles.be

Always discuss trial participation with your own doctor first.

Locations (21)

Hôpital Universitaire de BruxellesBrussels, BelgiumRecruiting
Universitair Ziekenhuis BrusselBrussels, BelgiumRecruiting
Centre Hospitalier Universitaire Marie CurieCharleroi, BelgiumRecruiting
Centre Hospitalier Chrétien - MontLégiaLiège, BelgiumRecruiting
Centre Hospitalier Universitaire Sart-TilmantLiège, BelgiumRecruiting
Centre Hospitalier Universitaire TivoliLouvière, BelgiumRecruiting
Centre Hospitalier Universitaire Saint-PierreOttignies, BelgiumRecruiting
Amsterdam University Medical CenterAmsterdam, NetherlandsRecruiting
Rijnstate HospitalArnhem, NetherlandsRecruiting
Amphia ZiekenhuisBreda, NetherlandsNot Yet Recruiting
Catharina HospitalEindhoven, NetherlandsRecruiting
Medical Spectrum TwenteEnschede, NetherlandsRecruiting

+ 9 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06549426