None listed
Conditions
Interventions
Drug : We meet the patient the day before the surgery is scheduled. Through the pre-anesthesia evaluation, we check the overall condition of the patient who can participate in the clinical trial, the
Sponsors
Chonnam National University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: American Society of Anesthesiologists Physical Status Classification (ASA PS) 1-4 patients Patients undergoing single heart valve surgery under general anesthesia: a mitral valve, aortic valve, or tricuspid valve Patients who voluntarily consented in writing to participate in this clinical study
Exclusion criteria
Exclusion criteria: Taking sleeping pills, antipsychotics, or narcotic pain relievers for more than 1 week physical disability illiteracy In case of conversion to surgery using an extracorporeal circulation device Left ventricular function (rescue fraction) less than 30% In case of major organ failure before surgery (Plasma creatine 2mg/dL or higher, AST/ALT 3 times higher than normal before surgery and there is a continuous increase, or there is a neurological abnormality) If mechanical ventilation assistance is continuously required after surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of differences in quality of recovery questionnaire (QoR-40K) scores at 24 hours after extubation between the two groups | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital signs (blood pressure, heart rate), amount of sufentanil administered during surgery, amount of fluid, amount of vasopressor, amount of blood products, timing of extubation after surgery, pain at the surgical site | — |
Countries
Korea, Republic of
Contacts
Public ContactJoungmin Kim
Chonnam National University Hospital
Outcome results
None listed