Accuracy Assessment of Exhaled Propofol Concentration Monitoring in Patients under General Anesthesia
Not Applicable
- Conditions
- Patient Undergoing Elective Surgery under General Anesthesia
- Registration Number
- JPRN-UMIN000036435
- Lead Sponsor
- Showa University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Contraindication to propofol or hydroxyethil starch administration (2) Obstructive and/or restrictive ventilatory impairment (3) American Society of Anesthesiologists physical status 4 or larger
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ratio of exhaled propofol cocentration versus plasma propofol concentration or an index simialr to the ratio during the general anesthesia
- Secondary Outcome Measures
Name Time Method 1. Ratio of measured propofol cocentration versus predicted plasma propofol concentration or an index simialr to the ratio during the general anesthesia 2. pharmacokinetic model to predict plasmaconcentration using exhaled propofol concentration