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Effect of Standard Laryngoscopy Versus Video-laryngoscopy

Not Applicable
Conditions
Difficult Intubation
Registration Number
NCT05902858
Lead Sponsor
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria
Brief Summary

The aim of this open-label, randomized, 3-parallel arm trial is to compare success of intubation rate at first try between three groups that will be intubated:

1. Conventional intubation with hyperangulated videolaryngoscope (control group),

2. Intubation ProVu TM video stylet combined with hyperangulated videolaryngoscope,

3. Intubation ProVu TM video stylet combined with standard Macintosh laryngoscope.

Detailed Description

Critical anesthetic incidents in the operating room are often related to airway management. Difficult airway management is defined as the clinical situation in which an anesthesiologist with conventional training has difficulty with upper airway face mask ventilation, difficulty with tracheal intubation, or both. Airway management has undergone a major transformation since the development of hyper-angle videolaryngoscopy (VL). Recently, the ProVuTM video stylet (Flexicare Medical Ltd, Mountain Ash, UK), which combines visualization technology with a tube guidance system, has been proposed as a new device for endotracheal intubation in participants with difficult airway management.

The investigators hypothesized that the ProVuTM video stylet combined with videolaryngoscopy or standard laryngoscopy may improve the success rate of intubation on the first attempt compared with using a videolaryngoscope alone in patientes with predicted difficult intubation. In fact, using ProVuTM the position of the video stylet tip can be adjusted continuously during the tracheal intubation maneuver.

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
114
Inclusion Criteria
  • patients undergoing elective surgery requiring oral tracheal intubation;
  • ≥18 years of age;
  • simplified Arné score ≥11;
  • Written informed consent will be obtained from every participant.
Exclusion Criteria
  • ≤18 years of age
  • interincisor distance at maximal mouth opening ≤2 cm;
  • planned awake fiberoptic intubation because patients are patients considered to be high-risk for difficult intubation or difficult mask ventilation (e.g. with neck tumours, complete cervical arthrodesis; neck circumference >50 cm);
  • patients at risk of gastric aspiration
  • planned nasal intubation.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Success rate on first intubation attempsDuring the procedure

The first-attempt intubation success is defined as tracheal tube placement with a single maneuver after insertion of the tube in the mouth. Reinsertion of the tube in the mouth counts as an additional attempt.

Secondary Outcome Measures
NameTimeMethod
Time of intubationDuring the procedure

Time from insertion of the laryngoscope beyond the dental rhyme to cuffed tube

Number of intubation attemptsDuring the procedure

Times of reinsertion of the tube beyond the dental rhyme

ComplicationsDuring the procedure

Evaluation of the type and rate of complications, including desaturation \< 90%, esophageal intubation, tooth breakage and bleeding from the oropharyngeal mucosa

Use of "jaw trust" or "BURP"During the procedure

Need to perform adjuvant maneuvers (jaw trust or BURP), measured with yes/no

Need of another anesthesiologist interventionDuring the procedure

Required intervention of another anesthesiologist, measured with yes/no, after 3 failed intubation attempt or after request of the first anesthesiologist

Needs to change the path of the intubation strategyDuring the procedure

Needs to change intubation strategy, measured with yes/no, includes use of fiberoptic intubation, change of videolaryngoscope or postpone intervention

Learning curve analysis of time of procedureThrough study completion, an average of 1 year

Improvement of time of procedure

Learning curve analysis of intubation rate successThrough study completion, an average of 1 year

Improvement of intubation rate success

Time of laryngoscopyDuring the procedure

Time from insertion of the laryngoscope beyond the dental rhyme to the insertion of the tube beyond the dental rhyme

Trial Locations

Locations (1)

Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo

🇮🇹

Alessandria, Piedmont, Italy

Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo
🇮🇹Alessandria, Piedmont, Italy

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