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Perfusion Index in Pediatric Low-Flow Anesthesia

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated July 10, 2025 (before its estimated August 5, 2025 completion). Its status may not reflect the trial's current state.

Record History

  1. Notable Trial status: Not Yet Recruiting to Recruiting Primary completion date: Sep 5, 2025 to Aug 5, 2025 · Completion date: Oct 5, 2025 to Aug 10, 2025 · Start date changed from estimate of Jun 5, 2025 to Jun 15, 2025 · 1 morev3 Show 4 more changesShow less
    • Primary completion date: Sep 5, 2025 to Aug 5, 2025
    • Completion date: Oct 5, 2025 to Aug 10, 2025
    • Start date changed from estimate of Jun 5, 2025 to Jun 15, 2025
    • Site details revised
  2. Notable Start date: May 5, 2025 to Jun 5, 2025v2
  3. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This study aims to evaluate changes in perfusion index (PI) in pediatric patients undergoing elective surgery under low-flow anesthesia. PI will be monitored at multiple intraoperative and postoperative time points to assess its relationship with hemodynamic stability and depth of anesthesia. The study will also investigate whether low-flow anesthesia affects the incidence of emergence agitation (EA). Patients will be assigned to either low-flow or normal-flow anesthesia groups based on routine clinical practice. No intervention will be applied beyond standard care. The findings are expected to provide insight into the predictive value of PI in postoperative recovery and support safer anesthesia practices in pediatric populations.
Trial Details
NCT Number NCT06967675
Lead Sponsor Istinye University
Conditions Perfusion Index, Low-Flow Anesthesia, Postoperative Recovery
Enrollment 90 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov