Patient undergoing scheduled surgery
Conditions
Interventions
None listed
Sponsors
Fukushima Medical University Department of anesthesia
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients undergoing scheduled surgery under general anesthesia and spinal anesthesia
Exclusion criteria
Exclusion criteria: Patients in reoperation, patients who could not obtain informed consent to the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The presence or absence of decrease in SpO2 within 48 hours after operation, respiratory complication, wound infection, cerebrovascular event, cardiovascular event, acute renal failure, suture failure, infection, re-intubation, death within 30 days , death within 60 days and death within 1 year and the artificial respiration period | — |
Countries
Japan
Contacts
Public ContactAsami Takagi
Fukushima Medical University Department of anesthesia
Outcome results
None listed