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Search / Trial NCT06549426

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

Launched by UNIVERSITY OF TWENTE · Aug 7, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

The TELSTAR-2 trial is a study aimed at understanding how to treat a specific type of brain activity called electrographic status epilepticus (ESE) in patients who are in a coma after a cardiac arrest. The main goals of the trial are to see if treating ESE can improve the recovery outcomes for these patients and to evaluate how this treatment affects healthcare costs. In this study, some patients will receive standard care along with anti-seizure medication, while others will only receive standard care without the medication.

To be eligible for the trial, participants must be at least 18 years old, in a coma after a cardiac arrest, and have specific findings on their brain monitoring (EEG) that suggest they have ESE. The trial is not yet recruiting participants, but it will involve patients from the Netherlands and Belgium. If someone qualifies and joins the study, they will receive close monitoring and care to help determine the best approach to treating their condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Coma (Glasgow Coma Scale score ≤ 8) after out of hospital cardiac arrest and resuscitation
  • 2. Age ≥ 18 years
  • 3. Continuous EEG with at least eight electrodes started \< 24h after return of spontaneous circulation (ROSC)
  • 4. ESE or possible ESE according to the Salzburg and ACNS criteria
  • 5. Possibility to start treatment within three hours after detection of ESE
  • Exclusion Criteria:
  • 1. Known history of another medical condition with limited life expectancy (\< six months)
  • 2. Any progressive brain illness, such as a brain tumor or neurodegenerative disease
  • 3. Pre-admission Glasgow Outcome Scale score of 3 or lower
  • 4. Reason other than the neurological condition to withdraw treatment
  • 5. EEG background activity prior to the emergence of ESE indicative of extensive irreversible anoxic brain injury
  • 6. Follow-up impossible due to logistic reasons, for example not living in the Netherlands or Belgium

About University Of Twente

The University of Twente is a leading research institution located in the Netherlands, renowned for its innovative approach to technology and health sciences. With a strong emphasis on interdisciplinary collaboration, the university conducts cutting-edge clinical trials that aim to advance medical knowledge and improve patient outcomes. Leveraging state-of-the-art facilities and a team of expert researchers, the University of Twente is committed to translating scientific discoveries into practical applications, fostering a dynamic environment for education and research that addresses pressing health challenges.

Locations

Leiden, , Netherlands

Arnhem, , Netherlands

Eindhoven, , Netherlands

Nieuwegein, , Netherlands

Groningen, , Netherlands

Gent, , Belgium

Genk, , Belgium

Brussels, , Belgium

Nijmegen, , Netherlands

Rotterdam, , Netherlands

Rotterdam, , Netherlands

Enschede, , Netherlands

Nijmegen, , Netherlands

Venlo, , Netherlands

Amsterdam, , Netherlands

Brussels, , Belgium

Brussels, , Belgium

Charleroi, , Belgium

Liège, , Belgium

Liège, , Belgium

Patients applied

0 patients applied

Trial Officials

Jeannette Hofmeijer, MD

Principal Investigator

University of Twente

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported