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Study identifier: NCT04170491 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

EEG Monitoring for Refractory Status Epilepticus

Condition: Status Epilepticus  ·  Sponsor: Barts & The London NHS Trust

PhaseNA
Planned participants40
Who can joinAll sexes, 16 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective randomized study to investigate the yield of continuous electroencephalogram (cEEG), as a diagnostic tool in intensive care unit (ICU), for patients with refractory status epilepticus (RSE) and the contribution of this test to the patient final outcome, compared with standard medical care. Specifically, the hypothesis is that the use of cEEG for patients with RSE will significantly reduce the length of in-hospital stay, mortality, and subsequent complications (such as infections or pressure ulcers). It is also predicted that quality of life will be higher following cEEG at 0, 3, 6 and 12 months after discharge. As there are currently no data available from previous studies assessing the impact of cEEG on markers of the final clinical outcome in patients with RSE, this study is going to start as a feasibility study, aiming to obtain initial data for the primary outcome measure, in order to perform a sample size calculation for a larger future trial. The pilot study will also assess the integrity of the study protocol, specifically the recruitment process and the consent procedure, and also determine the necessary costs for running a cEEG service in ICU for patients with RSE

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

Talk to the study team

Vasiliki Tsirka, Consutlant  ·  00447407781374  ·  vasiliki.tsirka@nhs.net

Always discuss trial participation with your own doctor first.

Locations (1)

Royal London HospitalLondon, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT04170491