None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 20 years or older Patients scheduled to undergo carotid endarterectomy under general anesthesia Patients with an American Society of Anesthesiologists (ASA) Physical Status classification of I to III Patients with a body weight of 40 kg or higher Patients who voluntarily provided written informed consent to participate in this clinical study
Exclusion criteria
Exclusion criteria: Patients with hemoglobin < 9 g/dL Patients with an estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m² Patients who donated 450 mL or more of whole blood within 30 days prior to screening Patients who experienced an acute illness likely to cause dehydration within 3 days prior to fluid infusion (for example, diarrhea or acute gastrointestinal illness) Patients deemed unsuitable for study participation at the investigator’s discretion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| hemoglobin;hematocrit | — |
Secondary
| Measure | Time frame |
|---|---|
| Type and total volume of intraoperative fluids administered;Dose and timing of intraoperative vasopressors and vasoconstrictors administered;Intraoperative urine output and estimated blood loss;Intraoperative anesthetic hemodynamic values (blood pressure, heart rate);Intraoperative anesthetic agents | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center