CompletedNot Applicable

TELSTAR: Treatment of ELectroencephalographic STatus Epilepticus After Cardiopulmonary Resuscitation

Belgium, Netherlands172 participantsStarted 2014-04

Plain-language summary

The purpose of this study is to estimate the effect of medical treatment of electro-encephalographic status epilepticus on neurological outcome of patients with postanoxic encephalopathy after cardiac arrest.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients after cardiac arrest with suspected postanoxic encephalopathy * Age 18 years or older * Continuous EEG with at least eight electrodes started within 24 hours after cardiac arrest * Electroencephalographic status epilepticus on continuous EEG * Possibility to start treatment within three hours after detection of electroencephalographic status epilepticus. Exclusion Criteria: * A known history of another medical condition with limited life expectancy (\<6 months) * Any progressive brain illness, such as a brain tumor or neurodegenerative disease * Pre-admission Glasgow Outcome Scale score of 3 or lower * Reason other than neurological condition to withdraw treatment * Follow-up impossible due to logistic reasons

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Neurological outcome

Timeframe: three months

Trial details

NCT IDNCT02056236

SponsorUniversity of Twente

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-04-24

View on ClinicalTrials.gov More Cardiac Arrest trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.