The patients planned lung or esophageal surgery
Conditions
Interventions
The group that undergone total intravenous anesthesia with propofol and remifentanil. Our study will be continued for 2 days.
The group that undergone general anesthesia with desflurane and remifenta
Sponsors
Sapporo Medical University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The patients planned lung or esophageal surgery
Exclusion criteria
Exclusion criteria: The patients that has difficulty in mutual understanding or disagree about this study or cannot be used propofol and desflurane
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The relative change of brain regional saturation of oxygen between pre-one lung ventilation and post-that. | — |
Countries
Japan
Contacts
Public ContactTakada Hiroshi
Hospital section clinical study section
Outcome results
None listed