Required propofol dose and time to emerge for anesthesia, affect by antiepileptics and disability
Not Applicable
- Conditions
- patients with neurological disorder who were treated under intravenous general anesthesia
- Registration Number
- JPRN-UMIN000012882
- Lead Sponsor
- Kagoshima university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
Not provided
Exclusion Criteria
The cases that did not use TCI and BIS or did not consent of study were excluded.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method We measure predictive blood concentration, time for emergence and propofol dose.
- Secondary Outcome Measures
Name Time Method