None listed
Conditions
Interventions
None listed
Sponsors
Chosun University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Total intravenous anesthesia using propofol and remifentanil. Adults over 20 years old American Anesthesia Society Physical classification grades I, II, and III Patients who voluntarily agreed to participate in this clinical study
Exclusion criteria
Exclusion criteria: Patients with over 30 of body mass index Patients with aortic valve insufficiency Patients with a forehead skin condition that is not suitable for attaching a sensor of a cerebral oxygen saturation monitoring device
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cerebral oxygenation | — |
Secondary
| Measure | Time frame |
|---|---|
| Arterial pressure (systolic, diastolic, mean) and heart rate, peripheral oxygen saturation, end-tidal carbon oxide fraction, anesthesia depth, mechanical ventilation parameters (tidal volume, respiratory rate, positive end-expiratory pressure, peak airway pressure, plateau airway pressure, and pulmonary compliance) ;Arterial blood gas analysis ;Demographic data of patients;Preoperative pulmonary function test | — |
Countries
Korea, Republic of
Contacts
Public ContactSang Hun Kim
Chosun University Hospital
Outcome results
None listed