Status:
COMPLETED
Sedation Monitoring Using Frontal Electroencephalogram, Electromyogram and Hemodynamic Responses to Pain in Critical Care
Lead Sponsor:
University of Helsinki
Conditions:
Electroencephalography
Critical Care
Eligibility:
All Genders
18+ years
Brief Summary
Purpose: Assessing nociception and sedation in mechanically ventilated patients in the ICU is challenging, with few reliable methods available for continuous monitoring. Measurable cardiovascular and ...
Eligibility Criteria
Inclusion
- Adult patients (over 18 years old)
- Postoperative ICU admission (planned and un-planned admissions), on mechanical ventilation via an endotracheal tube, with invasive hemodynamic monitoring via an arterial line
- receiving intravenous sedation by continuous infusion (propofol, midazolam).
Exclusion
- primary neurological disorders (including stroke, cardiac arrest with probable hypoxic brain injury, intracranial hemorrhage, and head injury with reduced level of consciousness prior to intubation), the continuous use of neuromuscular blocking agents during monitoring, confirmed meningitis or encephalitis, or a short data collection time (less than 12 hours).
Key Trial Info
Start Date :
May 7 2007
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 1 2009
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT04472247
Start Date
May 7 2007
End Date
April 1 2009
Last Update
July 15 2020
Active Locations (2)
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1
Helsinki University Central Hospital, Department of Anesthesiology and Intensive Care
Helsinki, Uudenmaan Lääni, Finland, 00029
2
Helsinki University Central Hospital, Department of Cardiac Surgery
Helsinki, Uudenmaan Lääni, Finland, 00029