Pleth Variability Index Monitoring in Pediatric Craniosynostosis Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 6
SponsorMuzaffer GENCER

About this trial

This prospective observational study aims to evaluate the role of pleth variability index (PVI) and perfusion index (PI) monitoring in intraoperative hemodynamic control among pediatric patients undergoing craniosynostosis surgery. Patients aged 0-6 years will be monitored intraoperatively using standard anesthesia monitoring together with PVI and PI measurements. Hemodynamic parameters, including systolic, diastolic and mean arterial pressure, heart rate, central venous pressure, oxygen saturation, body temperature, urine output, blood loss, fluid replacement, blood product requirement, serum lactate level, blood gas parameters and intraoperative complications will be recorded. The study will assess the association between PVI/PI changes and intraoperative hemodynamic status, bleeding and transfusion requirements.

Eligibility criteria

Qualifiers

Pediatric patients aged 0 to 6 years

Patients scheduled to undergo craniosynostosis surgery

American Society of Anesthesiologists physical status I, II or III

Written informed consent obtained from the parent or legal guardian

Disqualifiers

Patients older than 6 years

American Society of Anesthesiologists physical status IV

Inappropriate preoperative fasting status

History of significant cardiac, pulmonary or renal disease

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

30 Participants
are grouped into 1 trial group

Sponsors and collaborators

Muzaffer GENCER

Lead sponsor

Başakşehir Çam & Sakura City Hospital

Sponsor institution

Başakşehir Çam & Sakura City Hospital

Collaborator