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Comparison Between a Standard Tube and the Ultra-thin Tritube for Intubation of the Trachea and for Maintaining Access to the Trachea After Anaesthesia, in Patients With an Expected Difficult Direct Laryngoscopy

Sammenligning Mellem Standard Tube og Den Ultra-tynde Tritube® Til Intubation, og Til Opretholdelse af Adgang Til Trachea Efter anæstesi, Hos Patienter Med Forventet Vanskelig Direkte Laryngoskopi

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03653039
Acronym
Tritube
Enrollment
48
Registered
2018-08-31
Start date
2018-09-12
Completion date
2019-02-14
Last updated
2024-02-29

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

Conditions

Larynx Cancer, Oral Neoplasm, Pharynx Cancer

Brief summary

The investigators compare the ease of intubation between a new ultra-thin endotracheal tube, Tritube, and a standard endotracheal tube in patients with predictors of difficult laryngoscopy. Furthermore the investigators compare the acceptance of leaving the Tritube in trachea after end of anaesthesia, with the use of a tube exchange catheter.

Detailed description

In patients scheduled for surgery and anaesthesia in the Head-/neck/ear/nose/throat -region the investigators compare the ease of tracheal intubation between a new ultra-thin endotracheal tube, Tritube, and a standard endotracheal tube in patients with predictors of difficult laryngoscopy. The intubation is performed with an angulated video laryngoscope. Furthermore the investigators compare the acceptance of leaving the Tritube in trachea after end of anaesthesia, with the use of a tube exchange catheter. The latter continues into the post-operative recovery-ward.

Interventions

DEVICETritube

The ultra thin tribute is used used for the ventilation of the patients in this arm

DEVICEStandard enditracheal tube

A standard endotracheal tube is used used for the ventilation of the patients in this arm

Sponsors

Michael Seltz Kristensen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Randomised controlled

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients for anaesthesia for surgery in the Head-/neck/ear/nose/throat * planned for oral intubation with video-laryngoscopy * with risk factors for difficult direct laryngoscopy

Exclusion criteria

* Patient with increased secretions in the airway (Pneumonia, bronchitis, productive cough) * Patients planned for awake intubation * Patients where mask-ventilation is judged to could become impossible * Patients where access to the cricothyroid membrane is judged to be difficult or impossible * Patients in ASA (american Society of Anaesthesiologists) physical classification status \>3 * Patients who are scheduled for rapid sequence induction (RSI) due to risk of aspiration * Patients with stridor * Patients with hypoxemia (Saturation \< 90 % in room air) * Operation duration planned to \> 2.5 hours * Patients with the need for a nerve-stimulation-tube during surgery

Design outcomes

Primary

MeasureTime frameDescription
Rate of Excellent intubation conditions2 hoursRate of Excellent intubation conditions judged on the scale excellent/good/fair/poor

Secondary

MeasureTime frameDescription
The Intubation Difficulty Score (IDS)2 hoursThe intubation difficulty scale , range 0 to 7, 0 indicates easy intubation, 1 - 5 indicates slight difficulty, 5\< indicates moderate to major difficulty
Time to intubated2 hoursTime from the tube is advanced past the vocal cords until the cuff is inflated in the trachea
Time to the patient becomes ventilated via the tube2 hoursTime from the tube is advanced past the vocal cords until the cuff is inflated in the trachea and CO2 waveform is observed
Number of intubation attempts2 hoursone attempt is every-time the tube is advanced past the incisors
The rate of succesful intubation with 60 seconds1 minute
Number of remodellings of the stilette2 hours
rate of use for reverse loading of the tube on the stylet2 hours
the percent of glottic opening , (POGO), Before the tube is inserted2 hours
The rate of interruption by the tube of the view to the vocal cords at any time, to such a degree that it disturbs the intubation2 hours
Intubation conditions Strom scale2 hoursDirection of the tube-stylet combination excellent/good/poor, easy/fair/difficult. Advancement of the tube-stylet combination excellent/good/poor easy/fair/difficult
The surgeons score of the space and working conditions in the mouth/pharynx and larynx after intubation2 hours
The difference between ET CO2 and arterial blood-gas CO2 after 15 minutes of surgery20 minutes
the duration of the Tritube being in the trachea after return of spontaneous ventilation and deflation of the cuff /(Tritube group)4 hours
The duration of the tube-exchange catheter being in the trachea after its placement / (Tube-exchange-catheter group)4 hours
The ration of patients who still has the Tritube or the tube-exchange-catheter in place when arriving in the post-operative recovery unit4 hours
The ration of patients who still has the Tritube or the tube-exchange-catheter in place one hour after arrival in the Post anaesthesia care unit the post-operative recovery unit4 hours
The patient's satisfaction with having the Tritube or the tube-exchange-catheter in place when being awake in the Post anaesthesia care unit4 hoursVisual analog scale from 1-10, 1= no nuisance, 10= unberable
thepercent of glottic opening , POGO, with the tube in place2 hors

Countries

Denmark

Outcome results

None listed

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