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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Trial Officials
Jeannette Hofmeijer, MD
Principal Investigator
University of Twente
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported