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OpenTrials
Completed

NCT Number: NCT02016144

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

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

Completed

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Key information

Age range

20 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Seoul National University Dental Hospital

Seoul, 110-768, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. optimal length of pre-inserted ETT for nasal fiberoptic intubation

    Time frame: during endotracheal intubation for general anesthesia

Sponsors and collaborators

Lead sponsor

Seoul National University Dental Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Dec 19, 2013
Registry last updated
Dec 19, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.