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Clinical Trial

Comparison of First Attempt Success Based on Endotracheal Tube Type During Videolaryngoscope-guided Intubation Without Stylet

NCT: NCT07682480 · NOT_YET_RECRUITING

NCT IDNCT07682480
StatusNOT_YET_RECRUITING
Start Date2026-12-01
Completion2028-04-17
SponsorSeoul National University Hospital (OTHER)
First posted
Last updated

Brief Summary

Patients are randomly assigned to either the oral RAE tube group (Group O) or the reinforced tube group (Group R). In both groups, tracheal intubation is performed using a videolaryngoscope without a stylet, and the first-attempt success rate is compared. Upon emergence from anesthesia and removal of the endotracheal tube, the degree of subglottic injury is assessed and compared between the groups. In addition, postoperative sore throat and hoarseness are evaluated and compared at 1 hour and 24 hours after surgery.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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