Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05263674

Fast Acute Sedation at Intensive Care vs. High-dose i.v. Anti-seizure Medication for Treatment of Non-convulsive Status Epilepticus (FAST-trial)

This open-label, randomized multicenter trial aims at clarifying the standard of care of patients with non-convulsive status epilepticus not responding to treatment with benzodiazepines and at least one high-dose intra venous anti-seizure medication.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–120 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Aarhus Universitetshospital, Aarhus, Denmark

Loading trial locations.

About this study

Persistent epileptic seizures, aka. status epilepticus (SE), are the second most common neurological cause of acute admissions. Around halv of the patients suffers from SE without prominent visible seizures ("convulsions"), which is referred to as non-convulsive status epilepticus (NCSE) and is afflicted with a long-term mortality of >50% also in patients without concomittant acute brain disease. There are no evidence-based treatment guidelines for NCSE but patients usually receive treatment with benzodiazepines followed by i.v. anti-seizure medication. If seizures continues, further treatment is controversial. The participating centers have long-standing experience in treating NCSE but use different, internationally accepted treatment strategies. Some initiate aggressive treatment with fast sedation at intensive care aiming at immediate seizure control, other estimate that the side effects of sediation does not outweigh the potential benefit and try high-dose i.v. anti-seizure medication that only slightly impair conciousness - often with success.

This randomized, open label, multicenter trial (Eudract 2021-003392-34) aims at clarifying the treatment of patients with NSCE not responding to standard therapy. Patients with verified NCSE based on clinical parameter or using electroencephalography (EEG) are randomized into a fast acute sedation group and a group that receives at least one additional, high-dose anti-seizure mediciation.

Primary objective endpoint is treatment failure 24 h after randomization as determined by EEG. Secondary endpoints are e.g. seizure-induced neurological damage, treatment-related complications and neurological long-term outcome.

The statistical planing aims at showing superiority of aggressive treatment, 140 patients shall be included in a three years period at the University Hospitals in Aarhus, Odense, Roskilde and Copenhagen.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients (older than 18 years) with EEG-verified NCSE, according to the Salzburg criteria, who have not responded to appropriate treatment with benzodiazepines and at least one 2nd line i.v. anti-seizure medication according to the current Danish national neurological treatment guidelines (Levetiracetam, Fosfenytoin or Valproate).

Exclusion criteria

  • patients with epilepticus status due to acute neuroinfection (e.g. bacterial meningitis or viral encephalitis)
  • acute traumatic or spontaneous intracranial hemorrhage
  • suspicion of cerebral anoxia / hypoxia / hypoglycemia / epileptic encephalopathy
  • contraindications to anti-seizure medication defined in the protocol
  • contraindications to anesthesia treatment in intensive care
  • focal motor status epilepticus without relevant conscious influence (Glasgow Coma Scale> 13)
  • known epileptic encephalopathy
  • Clinical need for acute intubation

Treatment and study plan

Rapid sedation

Drug

High-dose Propofol (bolus 3-5 g / kg, maintenance dose 5-10 mg / kg / hour) to - 5 on the Richmond agitation sedation scale (RASS) for 20 hours, and a single anti-epileptic drug should be added as adjunctive therapy. Addition of low-dose Midazolam (max. 0.1 mg / kg / h) is permitted if deep sedation (defined clinically by RASS -5) is not possible with Propofol alone.

Primary outcomes

  1. Proportion of patients with continued NCSE on EEG after 24 h ("treatment failure")

    Time frame: 24 hours after randomisation

    NCSE diagnosed using EEG and defined by the "Salzburg criteria" for NCSE (e.g. Leitinger et al. Lancet Neurology, 2016)

Secondary outcomes

  1. Number of treatment related complications

    Time frame: at discharge, on average after 7 days

    e.g. tracheostoma, infections

  2. New neurological deficit

    Time frame: at discharge, on average after 7 days

    Neurological deficits are quantified using National Institute of Health Stroke Scale (NIHSS, maximum possible score is 42, the minimum score - indicating no deficits - is 0) at admission and discharge. New neurological deficit is defined as increase of NIHSS >5 at discharge

Other outcomes

  1. Influence of cEEG on new neurological deficit

    Time frame: at discharge, on average after 7 days

    Patients receive either cEEG or spot EEG depending on the center. In this pre-specified analyses, the impact of cEEG vs. spot-EEG on the degree of new neurological deficits (outcome 3) will be compared

  2. Duration of intensive care treatment

    Time frame: at discharge, on average after 7 days

    Definition: Time from intubation to discharge from ICU

  3. Duration of hospitalization

    Time frame: 1-100 days, on average 7 days

    Time from randomization to discharge from hospital in charge for acute treatment of NCSE

  4. Proportion of patients with superrefractory status epilepticus

    Time frame: at discharge, on average after 7 days

    Proportion of patients that develop superrefractory status epilepticus after randomization but during current hospitalization

  5. Survival after discharge

    Time frame: 3, 6, 12, and 24 months after randomization

    Determined at ambulatory control 3,6,12 and 24 months after randomization

  6. Quality of life after discharge

    Time frame: 3, 6, 12, and 24 months after randomization

    Determined using questionnaire/patient survey (Quality of Life in Epilepsy Inventory, Qolie-31 Danish translation), at ambulatory controls 3, 6, 12, and 24 months after randomization

Study contacts

Contact information is provided by the study sponsor or research team.

Christoph P. Beier, M.D.

CONTACT

[email protected]

+4565411943

Sponsors and collaborators

Lead sponsor

University of Southern Denmark

Other

Collaborators

  • Aarhus University Hospital
  • Copenhagen University Hospital, Denmark
  • University Hospital of Zealand

Registry information

Acronym: FAST

Important dates

Study start
2022
Primary completion
2027
Study completion
2028
First posted
Mar 2, 2022
Registry last updated
May 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.