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Nostril Side on Epistaxis

The Effect of Nostril Side on Epistaxis During Nasotracheal Intubation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06605989
Enrollment
208
Registered
2024-09-20
Start date
2024-09-26
Completion date
2026-02-28
Last updated
2026-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nasotracheal Intubation

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.

Interventions

PROCEDURENasotracheal intubation

For nasotracheal intubation, the nasal RAE tube will be first inserted through the left nostril for patients in the left nostril side arm. For nasotracheal intubation, the nasal RAE tube will be first inserted through the right nostril for patients in the right nostril side arm.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER
SMG-SNU Boramae Medical Center
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
epistaxisduring nasotracheal intubationepistaxis due to nasotracheal intubation

Countries

South Korea

Contacts

CONTACTJung-Man Lee, M.D., Ph.D.
jungman007@gmail.com+82-2-870-2513
PRINCIPAL_INVESTIGATORJung-Man Lee, M.D.,Ph.D.

Seoul National University College of Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026