Advanced vs Standard Hemodynamic Monitoring During Propofol Sedation for ERCP: A Prospective Study

The aim of this study is to evaluate whether there is a difference in hemodynamic events requiring intervention between patients monitored with advanced hemodynamic monitoring using the MostCare system and those monitored with standard monitoring alone during propofol sedation for ERCP procedures.

Inclusion Criteria: * Adults aged 18 years and older * Patients with an ASA physical status score of III or higher scheduled for ERCP * Patients maintaining spontaneous respiration * Patients who have provided written informed consent Exclusion Criteria: * Patients requiring general anesthesia * Patients requiring mechanical ventilation * Patients unsuitable for arterial catheterization due to coagulopathy or local infection * Pregnant women * Patients who do not sign the informed consent form