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

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Phase changed: not specified → not applicablev5
  2. Study completion pushed from May 15, 2026 to Jul 15, 2026v4
  3. Re-verified, no change to tracked fieldsv3
  4. Site details revisedv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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 Details
NCT Number NCT07538115
Lead Sponsor Hitit University
Conditions
(from sponsor)		 Hemodynamic Instability
Enrollment 32 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov