Clinical Trial

A Nontraditional Approach for Awake Fiberoptic Nasotracheal Intubation.

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Record status
This record was last updated April 23, 2025 (before its estimated December 31, 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this clinical trial is to learn if awake nasotracheal fiberoptic intubation through an endotracheal tube inserted in the nasopharynx would be quick and have fewer complications than the conventional technique. The main questions it aims to answer are: which technique of intubation is faster, with more patient comfort and satisfaction? which technique has fewer complications like cough, bleeding, and laryngospasm? Researchers will compare intubation with the conventional fiberoptic technique for intubation to awake nasotracheal fiberoptic intubation through an endotracheal tube inserted in the nasopharynx. Participants will be monitored throughout the procedure for: 1. The duration of the intubation procedure 2. The mean peripheral oxygen saturation 3. Hemodynamic variables (HR, MAP)
Trial Details
NCT Number NCT06939998
Lead Sponsor Alexandria University
Conditions Endotracheal Tube Placement
Enrollment 112 participants
Start Date 2025-05-15
Primary Completion 2025-12-31 (estimated)
Study Completion 2025-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-04-23