drugset / Trial / NCT07680400

Propofol-sevoflurane Induction for Pediatric Nasotracheal Intubation.

NCT07680400

Not yet recruiting 160 enrolled Bezmialem Vakif University
RandomizedParallel-groupSingle-blindTreatment

Summary

Pediatric anesthesia differs significantly from adult anesthesia due to physiological differences and increased sensitivity to anesthetic agents. In surgeries requiring nasotracheal intubation, such as dental and maxillofacial procedures, achieving optimal intubation conditions while minimizing pharmacological exposure is of considerable importance. The combination of propofol and sevoflurane is frequently preferred in pediatric anesthesia because it provides rapid induction and stable hemodynamic conditions. Therefore, this randomized controlled trial aims to evaluate nasotracheal intubation conditions following propofol-sevoflurane induction with reduced pharmacological exposure in pediatric patients. The study is expected to contribute to clinical practice by enhancing patient safety while reducing anesthetic drug use.

Timeline

Start
2026-07-01
Primary completion
2026-08-01
Completion
2026-08-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Fentanyl Other / unclassified 1 ug/kg Intravenous
Comparator Rocuronium Other / unclassified 0.3 mg/kg Intravenous
Background Propofol Small molecule 2.5 mg/kg Intravenous
Background Sevoflurane Other / unclassified 8 % Inhaled

Indications

No indication recorded.