Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
500 participants
OBSERVATIONAL
2021-11-08
2025-06-09
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Ultrasound to Predict Difficult Airway
NCT03789071
Upper Airway Ultrasound Training Requirements
NCT05466409
Two Neck Ultrasound Measurements as Predictors of Difficult Laryngoscopy
NCT03547193
Sonographic Evaluation to Predict Difficult Airway Management
NCT03991325
Airway Ultrasound Assessment in the Prediction of Difficult Airway
NCT04816435
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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).
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
point of care ultrasound
Point of care ultrasound for upper airway evaluation.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Exclusion Criteria
* 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.
18 Years
99 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Ioannina
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Agathi Karakosta
Assistant Professor of Anaesthesiology
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Hospital of Ioannina
Ioannina, Epirus, Greece
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
768
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.