None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults aged 19 years or older Patients who require prolonged arterial pressure monitoring after general anesthesia and undergo arterial catheterization Individuals who have agreed to participate in the clinical trial and signed the informed consent form
Exclusion criteria
Exclusion criteria: Children under 19 years of age Patients in whom cannulation of both radial arteries is contraindicated (e.g., presence of AVF, history of injury, or failure to pass Allen’s test) Patients with peripheral arterial disease or moderate to severe valvular heart disease Individuals deemed by the investigator to be unsuitable for participation in the clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of overdamping | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of catheter insertion attempts;Number of oscillations generated after a fast flush while the wrist is fixed in extension following arterial catheter placement;Frequency of overdamping during surgery;Occurrence of overdamping according to patient position during surgery;Use of the wrist fixation device (CAS LL-03®, SH Medical, Republic of Korea) during arm immobilization;Satisfaction of anesthesiology nurses with intraoperative arterial line monitoring and management;Whether arterial blood pressure monitoring was interrupted due to arterial line malfunction during surgery;Whether arterial line malfunction occurred after transfer to the intensive care unit;Time of arterial line malfunction after transfer to the intensive care unit ;Whether overdamping occurs depending on the patient’s position in the intensive care unit ;Satisfaction of intensive care unit nurses with arterial blood pressure monitoring and management;Occurrence of postoperative complications (hematoma, vascular injury, or nerve injury) | — |
Countries
Korea, Republic of
Contacts
Samsung Medical Center