Electrophysiological Signatures of Cognitive Disorders Related to Intensive Care Unit (ICU) delirium_ BRAINSTORM-EEG
Key facts
- Who runs it
- University Hospital, Toulouse
- Where
- France1 site in 1 countryChoose a country to see its sites
- Trial code
- Status
- Terminated
- People taking part
- 8 people enrolled
- Started
- 21 May 2024
- Ended
- 25 Feb 2025
- Type of study
- Interventional, 2 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- mEEG battery
- Record updated
- 29 October 2026
- Why it stopped
- poor accrual
Who can take part
- Age
- 18 years to 80 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 14 criteriaShow less
Who can take part
- Patients admitted to the intensive care unit with ARDS (according to Berlin criteria)
- Membership of a social security scheme
- Signed consent of the patient (group without delirium) or referring person (group with delirium)
- Discontinuation of any sedative agent for ≥ 72 hours
Who cannot take part
- Previous neurological history
- Recent ICU admission (> 5 days of ICU hospitalization within 6 months prior to current ICU admission)
- Pre-existing psychotic disorders
- Pre-existing cognitive deficits
- Patients with chronic ethylism
- Patients whose delirium cannot be reliably assessed due to blindness, deafness or inability to speak French
- Patients whose life expectancy is unlikely to exceed 24 hours
- Pregnant women
- Patients under court protection
- Patients who have already participated in the study
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
Early cognitive assessment of critically-ill acute respiratory distress syndrome (ARDS) patients with delirium using a multidimensional electrophysiological evaluation battery (mEEG) to identify and characterize the neural correlates of cognitive dysfunctions associated with delirium (vigilance, attention, semantic and lexical processing, self-processing), and to develop a prognostic evaluation of neurocognitive and psychological disorders using an innovative non-behavioral approach.
The 2 groups in the trial
- Delirium patients groupTreatment being tested
Patients admitted for acute respiratory distress syndrome (ARDS) who developed delirium
Treatment: mEEG battery
- Patients without deliriumExisting treatment, for comparison
Patients admitted for acute respiratory distress syndrome (ARDS) who did not developed delirium
Treatment: mEEG battery
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Electrophysiological Signatures of Cognitive Disorders Related to ICU Delirium : a Pilot Study
- Record updated
- 29 October 2026