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NOT YET RECRUITING
NCT07680400
NA

Propofol-sevoflurane Induction for Pediatric Nasotracheal Intubation.

Sponsor: Bezmialem Vakif University

View on ClinicalTrials.gov

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.

Official title: Nasotracheal Intubating Conditions With Reduced Pharmacologic Exposure After Propofol-sevoflurane Induction in Pediatric Parients: a Randomized Contolled Trial

Key Details

Gender

All

Age Range

1 Year - 10 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2026-07-01

Completion Date

2026-08-01

Last Updated

2026-07-02

Healthy Volunteers

No

Interventions

DRUG

reduced pharmacologic exposure

patients in group R will undergo combination of sevoflurane and propofol only anesthesia induction

DRUG

conventional anesthetic induction

in group C, conventional anesthetic regimen will be used for anesthesia induction