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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHitit University

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Patients requiring general anesthesia

Patients requiring mechanical ventilation

Patients unsuitable for arterial catheterization due to coagulopathy or local infection

Pregnant women

Trial design

Treatments tested in this trial

  • Hemodynamic Monitoring
  • Standard Monitoring

Treatment groups

32 Participants
are divided into 2 treatment groups

Sponsors and collaborators