Advanced vs Standard Hemodynamic Monitoring During Propofol Sedation for ERCP: A Prospective Study
Recruiting
N/A
Interventional Study
Hemodynamic Instability
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 32 (estimated)
- Sponsor
- Hitit University · Other
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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.
Trial Locations
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Eligibility Criteria
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
* …
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