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

Recruiting now · Not applicable

Conditions studied: Hemodynamic Instability

In brief

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.

Key facts

Study ID

NCT07538115

Run by

Hitit University

People needed

32

Starts

2026-03-27

Expected to finish

2026-07-15

Last updated by the study team

2026-06-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Hitit university — Çorum, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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