RecruitingNot Applicable

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

Turkey (Türkiye)32 participantsStarted 2026-03-27

Plain-language summary

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.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Number of hemodynamic events requiring clinical intervention during ERCP under propofol sedation

Timeframe: From the start of sedation until the end of the ERCP procedure

Trial details

NCT IDNCT07538115

SponsorHitit University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-04-25

Contact for this trial

Sibel Onen Ozdemir, MD

+905442892194 sibelonen89@gmail.com

View on ClinicalTrials.gov More Hemodynamic Instability trials