At a glance
ClinicalIndex Comparison RecordN/ACompleted· 46 enrolled
Drug / intervention
SedLine EEG sensordevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
'Study of the Cerebral Effects of Sevoflurane, Propofol and Remifentanil as Measured by the Spontaneous Electro-encephalogram'
In Brief
A clinical study evaluating SedLine EEG sensor for Anesthesia. Completed, enrolled 46 participants across 1 site.
Detailed Summary
This is an interventional, randomized controlled study in health volunteers that involves collecting data on raw EEG waves measuring various combinations of anesthetic drugs during standardized drug titration.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAnesthesia
CountriesNetherlands
CollaboratorsUniversity Medical Center Groningen
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
Enrollment StartDec 2013
First PostedJan 2014
Primary CompletionJun 2015
TodayJul 2026
First PostedJan 23, 2014
Enrollment StartDec 16, 2013
Primary CompletionJun 4, 2015
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 12.4 years ago
Interventions
SedLine EEG sensordevice
Test subjects in each group will receive the same device intervention (SedLine EEG) to monitor their EEG waves.