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

NCT07538115 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 32

Last updated 2026-05-08

No results posted yet for this study

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.

Conditions

  • Hemodynamic Instability

Interventions

DEVICE

Hemodynamic Monitoring

Advanced hemodynamic monitoring performed using the MostCare system via radial arterial cannulation during ERCP under propofol sedation.

PROCEDURE

Standard Monitoring

Standard intra-procedural monitoring including non-invasive blood pressure, ECG, pulse oximetry, and BIS during ERCP under propofol sedation

Sponsors & Collaborators

  • Hitit University

    lead OTHER

Principal Investigators

  • Ozgur Yagan, Professor · Hitit University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-27
Primary Completion
2026-04-25
Completion
2026-05-15

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07538115 on ClinicalTrials.gov