Comparison of propofol and sevoflurane anesthesia: effects on change in ?O2Hbi, ?HHbi

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008073

Enrollment

100

Registered

2023-01-04

Start date

2023-02-17

Completion date

Unknown

Last updated

2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : The study director assigns the study subjects to either the sevoflurane group or the propofol group through a random assignment table. A random assignment table is prepared using a random numbe

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: He visited Eunpyeong St. Mary's Hospital and underwent surgery under general anesthesia, and a full-body image of the American Anesthesiology Association over the age of 70 Patients who fall under the placenta classification 1 and 2

Exclusion criteria

Exclusion criteria: ? Patients who are expected to experience difficult airways ? a patient with cognitive impairment (dementia, brain damage) ? If there is a tumor in the oral cavity or there is an abnormality in the structure ? Teeth shaking ? upper respiratory tract infection ? a patient with hemodynamic instability ? Patients whose electrocardiogram is not normal sinus rhythm on preoperative examination ? Unstable angina, left ventricular ejection fraction < 40% ? Severe vascular disease inserted pacemaker/defibrillator

Design outcomes

Primary

Measure	Time frame
?OxyHbi, ?HHbi difference according to rSO2 difference between Propofol and Sevoflurane	—

Secondary

Measure	Time frame
Non-invasive blood pressure, oxygen saturation (SpO2), electrocardiogram (ECG), PSI, PVI, PI, and anesthetic concentration at measurement time	—

Countries

Korea, Republic of

Contacts

Public ContactJi Young Min

The Catholic University of Korea

earlkain@naver.com+82-2-9371-7627

Outcome results