Pilot study for studying the influence of low-dose propofol on the classification of movements from the electroencephalogram in healthy participants
Completed
- Conditions
- perioperatieve monitoringmonitoring during anesthesia
- Registration Number
- NL-OMON38459
- Lead Sponsor
- niversitair Medisch Centrum Sint Radboud
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 12
Inclusion Criteria
-18-65 years old
-right-handed
-normal or corrected to normal vision
-normal or corrected to normal hearing
Exclusion Criteria
-neurological impairment
-motor disabilities
-known allergies or oversensitivity to propofol
-allergies to peanuts and/or soy
-cardiac respiratory, renal or hepatic impairment
-regular drug intake (of any kind, other than contraceptives and antihistamines)
-pregnancy or nursing
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie propofol's modulation of EEG movement classification in perioperative monitoring?
How does low-dose propofol compare to standard anesthetics in detecting movement artifacts via EEG during anesthesia?
Are specific EEG biomarkers predictive of propofol efficacy in distinguishing voluntary from involuntary movements during surgery?
What adverse events are associated with low-dose propofol use in EEG-based movement monitoring, and how are they managed?
What alternative anesthetic agents or EEG processing techniques synergize with propofol for improved movement detection in perioperative care?