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Airway ManagementNCT06701253

Upper Airway Ultrasound Evaluation

An observational study of Airway Management and Point of Care, run by University of Ioannina at 1 site in Greece.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Current guidelines support the use of predictive clinical tests in the evaluation of difficult airway, meaning either difficult bag and mask ventilation, conventional laryngoscopy and/or endotracheal intubation. Read more about this study

Who is it for?
Ages 18 to 99 yearsHealthy volunteers can take part
Conditions the study is for
Airway Management, Point of Care, Ultrasound
What is being tested?
point of care ultrasound
How many people
500 participants
Where
1 siteGreece
Study dates
8 Nov 2021to 9 Jun 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: General surgical population.

Who may be able to join

None listed.

Who cannot join

  • obstetric surgeries,
  • pregnancy,
  • non elective surgeries,
  • patients with previous surgeries involving the anterior surface of the neck (i.e., thyroid surgery),
  • patients with history of cervical radiation.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Greece1 site, 1 recruiting
  • University Hospital of Ioannina

    Ioannina, Epirus, 455 00

    Agathi Karakosta, 0030 2651099766, akarakosta@uoi.gr

    Danai Pantazi, 0030 2651099766, pantazidanai@hotmail.com

    Recruiting

Other trials in Greece

About this study

Official title: Ultrasound of the Anterior Neck Tissues, as a New Tool in the Evaluation of Difficult Airway.

Current guidelines support the use of predictive clinical tests in the evaluation of difficult airway, meaning either difficult bag and mask ventilation, conventional laryngoscopy and/or endotracheal intubation. However, despite the clinical use of these predictive tests, unpredictive difficult laryngoscopy complicates 1.5-13% of cases. Life threatening scenarios may be encountered in patients with difficult or impossible bag and mask ventilation.

Anaesthesiologists are familiar with the use of ultrasound, with peripheral nerve blockade and central vascular access representing the most popular applications during the last decades. The ultrasound provides real time and accurate images. According to the current literature, there are only a handful of studies relevant to the application of point of care ultrasound (POCUS), as a new tool in the upper airway evaluation. It is a new field of research with high interest.

Read more

This is a prospective observational study to investigate if specific ultrasound measurements of the anterior neck can serve as predictors of difficult airway. The ultrasound parameters will be measured preoperatively, during the preanaesthetic evaluation, along with standard clinical prognostic tools, like the mallampati score. The ultrasound parameters to be investigated are:

  1. the distance from thyroid isthmus to skin surface,
  2. the distance from the hyoid bone to the skin surface,
  3. the distance from the anterior commissure of vocal cords to the skin surface,
  4. the distance from skin to the trachea at the level of jugular notch,
  5. the distance from skin to epiglottis corresponding to half of the distance between thyroid cartilage and hyoid bone,
  6. and the angle between glottis and epiglottis. After the induction in anaesthesia, the Cormack Lehane score (grading of the laryngoscopy view) and the Han scale (grading of the degree of difficulty of bag and mask ventilation) will also be recorded.

The goal of this study is the investigation of the role of POCUS in the evaluation of difficult bag and mask ventilation and difficult intubation. The primary endpoint is the incidence of difficult bag and mask ventilation and the incidence of difficult laryngoscopy and intubation. Secondary endpoints are the correlations between clinical prognostic tools of difficult airway and the POCUS parameters under investigation.

Read the detailed description

Ultrasound of the anterior neck tissues, as a new tool in the evaluation of difficult airway.

Introduction The current guidelines provide predictive clinical tests in the evaluation of difficult airway, relevant to the mask ventilation, conventional laryngoscopy and endotracheal intubation. Despite similarities in predictors, the incidence of mask ventilation is distinct from difficult laryngoscopy and intubation, 7.8% and 12.3% respectively.

However, despite the clinical use of these predictive tests, unpredictive difficult laryngoscopy complicates 1.5-13% of cases. The risk of life-threatening complications is increased in patients with difficult or impossible bag and mask ventilation.

Anaesthesiologists are familiar with the use of ultrasound, with peripheral nerve blockade and central vascular access representing the most popular applications of the last decades. Ultrasound provides quick, easy and accurate images.

According to the current literature, there are a few studies relevant to the application of point of care ultrasound (POCUS), as a new tool in the upper airway evaluation. It is a new field of research with high interest.

This is a prospective observational study which is taking place at the University Hospital of Ioannina in order to investigate if some ultrasound measurements of the anterior neck can serve as predictors of difficult airway. The goal is to investigate the role of POCUS in the evaluation of difficult bag and mask ventilation and difficult intubation.

Aim of the study The primary outcome of this study is the incidence of difficult bag and mask ventilation and the incidence of difficult laryngoscopy and intubation.

Difficult bag and mask ventilation is defined as the inability of an unassisted conventionally trained anesthesiologist to maintain the oxygen saturation as measured by pulse oximetry > 92% or to prevent or reverse signs of inadequate ventilation during positive-pressure mask ventilation under general anesthesia.

Difficult intubation is when a conventionally trained anesthesiologist needs more than 3 attempts or more than 10 min to intubate the patient.

Secondary outcome is the investigation of the relationship between ultrasound parameters, Cormack- Lehane scale, Han scale and the clinical prognostic tools.

Secondary endpoints are the investigations of the relationships between standard clinical prognostic tools of difficult airway and the POCUS parameters under investigation.

Materials and Methods Anesthetic technique The ultrasound parameters will be measured in all the participants in the preanesthetic evaluation. The rest of anesthetic management will follow the standard practices and the protocols of our Anaesthesiology Department.

Data collection The collection of data concerns two time periods. The first, during the preanesthetic evaluation, when the standard clinical prognostic markers of difficult airway (Mallampati score, thyromental distance, sternomental distance, mouth opening, neck circumference, upper lip bite test, cervical mobility, presence of beard), as well as somatometrics (age, weight, height, gender and race) will be recorded. Moreover, the type of the operation, the physical classification of the American Society of Anesthesiologists physical status (ASA score) score, the comorbidities (by application of the Charlson Comorbidity Index) and the history of Obstructive Sleep Apnea (as evaluated by the Stop-Bang questionnaire) will also be recorded preoperatively.

Lastly, specific ultrasound markers of the anterior neck tissue will be evaluated preoperatively. This investigation will include the recognition and measurement of the following ultrasound parameters, either with the probe in the transverse or the sagittal axis:

  1. the distance from thyroid isthmus to skin surface (transverse axis),
  2. the distance from the hyoid bone to the skin surface (transverse axis),
  3. the distance from the anterior commissure of vocal cords to the skin surface (transverse axis),
  4. the distance from skin to the trachea at the level of jugular notch (transverse axis)
  5. the distance from skin to epiglottis corresponding to half of the distance between thyroid cartilage and hyoid bone (sagittal axis),
  6. and the angle between glottis and epiglottis (sagittal axis). The second period of data collection involves the post induction of general anaesthesia and intubation period. At this point the Cormack-Lehane score (grading of the laryngoscopy view), the Han scale (grading of the degree of difficulty of bag and mask ventilation), the total number of intubation attempts with conventional laryngoscopy, the number of the anesthesiologists involved and their level of experience, the use of auxiliary tools (McCoy laryngoscope, ESCHMANN bougie, forceps Magille, supraglottic devises, video laryngoscope, and other relevant tools), the kind and the size of the endotracheal tube and the outcome (successful conventional endotracheal intubation, postponing operation, front of neck access, etc.) will be recorded in detail.

Size sample and statistical analysis This is a prospective observational study. The sample size is calculated by the incidence of difficult intubation and laryngoscopy according to current literature. Specifically, the incidence of difficult intubation in the operation theatre varies between 1.15 up to 3.8% and the incidence of difficult laryngoscopy between 6.1 up to 13%.

Our aim is to include 60 cases in our study (10 per ultrasound parameter) with difficult intubation/laryngoscopy. To achieve this goal, we need to include 460 to 980 cases, based on the above-mentioned minimum and maximum reported incidences of difficult laryngoscopy. However, recruitment will be completed when at least 60 cases of difficult laryngoscopy and/or difficult intubation have been recorded.

The data analysis will be performed using the software Stata tm (Version 10.1 MP, Stata Corporation, College Station, TX 77845, USA).

Being tested
point of care ultrasound

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • point of care ultrasoundDiagnostic test

    Point of care ultrasound for upper airway evaluation.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of difficult intubation

    Difficult intubation is defined as requirement of more than three attempts with conventional laryngoscopy.

    Measured: From the beginning of the pre-oxygenation period up to securing the airway, with either up to 3 attempts of conventional laryngoscopy/intubation, or non-conventional intubation, or waking up the patient, whichever comes first.

  2. Incidence of difficult bag and mask ventilation

    Difficult mask ventilation is defined as the inability of an unassisted anesthesiologist to maintain the measured oxygen saturation as measured by pulse oximetry > 92% or to prevent or reverse signs of inadequate ventilation during positive-pressure mask ventilation under general anesthesia.

    Measured: From the beginning of the pre-oxygenation period up to securing the airway, with either up to 3 attempts of conventional laryngoscopy/intubation, or non-conventional intubation, or waking up the patient, whichever comes first.

Secondary outcomes (8)
  1. Cormack-Lehane classification

    Classifies laryngoscopy views obtained by direct laryngoscopy based on the structures seen (Grade I: visualization of the entire laryngeal aperture; Grade II: visualization of only the posterior commissure of the laryngeal aperture; Grade III: visualization of only the epiglottis; Grade IV: visualization of only the soft palate).

    Measured: From the beginning of the pre-oxygenation period up to the first, second or third attempt of conventional laryngoscopy, whichever comes first.

  2. Han scale classification

    Classifies the difficulty in bag and mask ventilation (Grade I: easy mask ventilation, Grade II: needs oral airway or adjuvant with or without neuromuscular blocking agents, Grade III: difficult - inadequate or unstable or requiring two care providers, with or without neuromuscular blocking agents, Grade IV: impossible - unable to mask ventilate with or without neuromuscular blocking agents).

    Measured: From the beginning of the pre-oxygenation period up to securing the airway, with either up to 3 attempts of conventional laryngoscopy/intubation, or non-conventional intubation, or waking up the patient, whichever comes first.

  3. Distance from thyroid isthmus to skin surface

    Ultrasound measurement of the distance from thyroid isthmus to skin surface with the probe in the transverse axis.

    Measured: 24 hours before elective surgery and general anaesthesia needing endotracheal intubation, during the pre-anesthetic visit.

  4. Distance from hyoid bone to skin surface

    Ultrasound measurement of the distance from hyoid bone to skin surface with the probe in the transverse axis.

    Measured: 24 hours before elective surgery and general anaesthesia needing endotracheal intubation, during the pre-anesthetic visit.

  5. Distance from anterior commissure to skin surface

    Ultrasound measurement of the distance from anterior commissure of vocal cords to the skin surface with the probe in the transverse axis.

    Measured: 24 hours before elective surgery and general anaesthesia needing endotracheal intubation, during the pre-anesthetic visit.

  6. Distance from trachea to skin surface

    Ultrasound measurement of the distance from trachea to skin surface at the level of jugular notch with the probe in the transverse axis.

    Measured: 24 hours before elective surgery and general anaesthesia needing endotracheal intubation, during the pre-anesthetic visit.

  7. Distance from epiglottis to skin surface

    Ultrasound measurement of the distance from epigottis to skin at the level of the thyrohyoid membrane with the probe in the sagital axis.

    Measured: 24 hours before elective surgery and general anaesthesia needing endotracheal intubation, during the pre-anesthetic visit.

  8. Angle between the epiglottis and glottis

    Ultrasound measurement of the angle between epiglottis and glottis at the level of thyrohyoid membrane with the probe in the sagital axis.

    Measured: 24 hours before elective surgery and general anaesthesia needing endotracheal intubation, during the pre-anesthetic visit.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Nov 2024
  2. Study start8 Nov 2021
  3. Primary completion18 Nov 2027 (estimated)
  4. Study completion9 Jun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06701253
Sponsor's protocol ID
768
Status last verified
May 2026
First submitted
3 Nov 2024
Last updated
4 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Airway Management and Point of Care, run by University of Ioannina at 1 site in Greece.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 4 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Greece. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Agathi Karakosta (0030 2651099766, akarakosta@uoi.gr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of difficult intubation (time frame: From the beginning of the pre-oxygenation period up to securing the airway, with either up to 3 attempts of conventional laryngoscopy/intubation, or non-conventional intubation, or waking up the patient, whichever comes first.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 May 2026.

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