Tube 1st Technique for Easy Fiberoptic Intubation

Sponsor
Ain Shams University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05399147
Collaborator
(none)
40
2
4

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: fiberoptic intubation classic technique
  • Other: fiberoptic intubation tube 1st technique
N/A

Detailed Description

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].

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Diagnostic
Official Title:
Tube First Technique as a Conduit for Easy and Fast Firberoptic Intubation
Anticipated Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: classic group (CL group)

20 patients will be enrolled to be intubated using the classic usual technique

Other: fiberoptic intubation classic technique
classic fiberoptic intubation

Other: tube 1st group (TF group)

20 patients will be enrolled to be intubated using the tube 1st technique

Other: fiberoptic intubation tube 1st technique
tube 1st technique

Outcome Measures

Primary Outcome Measures

  1. time 1 [baseline]

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

Secondary Outcome Measures

  1. other measures [baseline]

    1. total dose of propofol during procedure measured in mg

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Age between 20 and 60 years,

  2. ASA Class I& II,

  3. Maxillofacial surgeries ex: mandibular surgery, orthognathic surgery and dental extraction surgery,

  4. Other surgeries like: oral graft surgery, facial trauma, limited mouth opening ex: submandibular and facial abscess.

Exclusion Criteria:
  1. Patient's refusal,

  2. ASA III or more,

  3. Intrinsic and idiopathic coagulopathy,

  4. known allergy to any of the study medications,

  5. furthermore, patients were excluded if they had severe hypoxemias due to sever cardiac or lung disease

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Ain Shams University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Amr Gaber, lecturer, Ain Shams University
ClinicalTrials.gov Identifier:
NCT05399147
Other Study ID Numbers:
  • fiberoptic intubation
First Posted:
Jun 1, 2022
Last Update Posted:
Jun 1, 2022
Last Verified:
May 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 1, 2022