patients with neurological disorder who were treated under intravenous general anesthesia
Conditions
Interventions
None listed
Sponsors
Kagoshima university
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The patient that an agreement was provided
Exclusion criteria
Exclusion criteria: The cases that did not use TCI and BIS or did not consent of study were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| We measure predictive blood concentration, time for emergence and propofol dose. | — |
Countries
Japan
Contacts
Public ContactKentaro OUCHI
Kagoshima University Anesthesia center
Outcome results
None listed