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OpenTrials
Completed

NCT Number: NCT05399147

Tube 1st Technique for Easy Fiberoptic Intubation

the aim of this work is to study how this technique will make nasal fiberoptic intubation easier and faster than the usual classic technique

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Key information

Age range

20 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ain Shams University

Cairo, Egypt

About this study

Difficult intubation is one of the most significant issues anesthesiologists deal with, occasionally. Among these, mandibulofacial deformities face the biggest challenge in intubation and make an anticipated difficult airway (1), due to short length of mandible (HLM), short thyromental distance (TMD), short inter horizontal -incisors gap (IIG) and high grade modified Mallampati test (MMT) (2).

There are several strategies to approach these patients and each technique has unique benefits that should be used on experience. Sitting endotracheal intubation is a useful technique for airway control, in patients with difficult airway or in patients in whom maintenance of the upright posture is beneficial (3), A difficult airway is defined as difficulty with facemask ventilation, difficulty with tracheal intubation, or both (3). According to new updates on difficult airway management, by the American Society of Anesthesiologists, there are non-invasive and invasive interventions for the management of difficult airway. Non-invasive interventions include, without being limited to: awake intubation, video-assisted laryngoscopy, intubating stylets or tube-changers, supraglottic airway (SGA) for ventilation (e.g., LMA, laryngeal tube), SGA for intubation (e.g., ILMA), rigid laryngoscopic blades of variousdesign and size, fiberoptic-guided intubation, and lighted stylets or light wands, while invasive interventions include surgical or percutaneous airway, jet ventilation and retrograde intubation (4).

Attaching a nasal airway to a breathing circuit as a tool to assist or control ventilation is a very helpful trick to have in challenging airway management situations.

Typically, Fiberoptic bronchoscope is passed through the more patent nostril to follow the major nasal pathway at the floor of the nose along the superior aspect of the hard palate, the lateral aspect of the nasal septum inferior to the lower turbinate to reach the nasopharynx where the operator identifies the pharyngeal structures, such as the base of the tongue and/or the epiglottis that are mostly "in-fall" precluding clear views of the larynx requiring a jaw thrust to visualize the laryngeal structures for patients planned to be intubated under general anesthesia [5,6].

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age between 20 and 60 years,
  • ASA Class I& II,
  • Maxillofacial surgeries ex: mandibular surgery, orthognathic surgery and dental extraction surgery,
  • Other surgeries like: oral graft surgery, facial trauma, limited mouth opening ex: submandibular and facial abscess.

Exclusion criteria

  • Patient's refusal,
  • ASA III or more,
  • Intrinsic and idiopathic coagulopathy,
  • known allergy to any of the study medications,
  • furthermore, patients were excluded if they had severe hypoxemias due to sever cardiac or lung disease

Treatment and study plan

fiberoptic intubation classic technique

Other

classic fiberoptic intubation

fiberoptic intubation tube 1st technique

Other

tube 1st technique

Primary outcomes

  1. time 1

    Time frame: baseline

    time 1 = time from start from start of introducing the bronchoscope till viewing the vocal cord measured in seconds.

Secondary outcomes

  1. other measures

    Time frame: baseline

    • total dose of propofol during procedure measured in mg

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

Tube First Technique as a Conduit for Easy and Fast Firberoptic Intubation

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jun 1, 2022
Registry last updated
Oct 14, 2022

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.

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