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Optimal Length of Pre-inserted ETT for Nasal Fiber Optic Intubation

Optimal Length of the Pre-inserted Endotracheal Tube for Obtaining Good View of Laryngeal Opening for Nasal Fibreoptic Intubation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02016144
Enrollment
150
Registered
2013-12-19
Start date
2012-10-31
Completion date
2013-12-31
Last updated
2013-12-19

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

Conditions

Nasal Fiberoptic Intubation

Keywords

Airway management; Fiber optic technology; Intubation

Brief summary

This study is intended to find the optimal length of pre-inserted ETT for nasal fiberoptic intubation and the equation to predict it.

Interventions

None listed

Sponsors

Seoul National University Dental Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* ASA physical status I-II * aged 20-65 yr (adults)

Exclusion criteria

* rhinitis * bleeding diatheses * requirement of awake intubation * a previous major oral and maxillofacial surgery history * anatomical deformity of the face, neck and upper airway

Design outcomes

Primary

MeasureTime frame
optimal length of pre-inserted ETT for nasal fiberoptic intubationduring endotracheal intubation for general anesthesia

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026