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Clinical Trials/NCT06605989
NCT06605989RecruitingNot Applicable

The Effect of Nostril Side on Epistaxis During Nasotracheal Intubation

Seoul National University Hospital2 sites in 1 country208 target enrollmentStarted: September 26, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
208
Locations
2
Primary Endpoint
epistaxis

Study Overview

Brief Summary

The purpose of the study is to investigate the effect of the nostril side on epistaxis during nasotracheal intubation.

Detailed Description

This prospective randomized controlled study was approved by the IRB of our institute.

Patients requiring nasotracheal intubation will be screened for eligibility for the study. Then, patients will be randomized to one of two groups; (Group I: tube will be inserted through the left nostril and advanced into the oral cavity / Group II: tube will be inserted through the right nostril and advanced into the oral cavity). After induction of anesthesia and muscle relaxation, the preformed nasal RAE (Ring-Adair-Elwyn) tube will be inserted via the nostril, which is assigned to each patient according to the group, approximately 3-4 cm. Next, an anesthesiologist will advance the tube into the oral cavity. After the tube is placed in the oral cavity, the anesthesiologist will perform nasotracheal intubation with Magill forceps. After that, an investigator will check the occurrence of epistaxis due to nasotracheal intubation and its severity with a fiberoptic bronchoscope. After obtaining all data, investigators will analyze the incidence of epistaxis and its severity between the two groups.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Care Provider)

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • adult patients requiring nasotracheal intubation for elective surgery

Exclusion Criteria

  • refuse to participate in the study
  • severe deformity in the nose
  • current severe epistaxis
  • cannot insert the tube into a specific nostril side due to any reason

Arms & Interventions

left nostril side

Experimental

For nasotracheal intubation, the nasal RAE tube will be inserted through the left nostril and advanced into the oral cavity.

Intervention: Nasotracheal intubation (Procedure)

right nostril side

Experimental

For nasotracheal intubation, the nasal RAE tube will be inserted through the right nostril and advanced into the oral cavity.

Intervention: Nasotracheal intubation (Procedure)

Outcomes

Primary Outcomes

epistaxis

Time Frame: during nasotracheal intubation

epistaxis due to nasotracheal intubation

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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