- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07309978
Assessment Of Difficult Airway Predictors: A Prospective Comparison Of Upper Airway Ultrasound And Conventional Anthropometric Measures
March 6, 2026 updated by: Sami Eksert, Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
This prospective observational study aims to evaluate whether upper airway ultrasound measurements can improve the prediction of difficult airway compared with conventional anthropometric assessments.
Adult patients undergoing elective procedures requiring airway management will be included.
Ultrasound parameters such as tongue thickness, anterior neck soft tissue thickness, and hyomental distance will be measured before airway intervention.
Standard clinical predictors (Mallampati score, thyromental distance, neck circumference, etc.) will also be recorded.
The primary objective is to determine the diagnostic accuracy of ultrasound-based measurements in predicting difficult laryngoscopy and intubation.
The study seeks to provide evidence supporting the integration of upper airway ultrasound into routine pre-anesthetic airway evaluation.
Study Overview
Status
Recruiting
Study Type
Observational
Enrollment (Estimated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ankara, Turkey (Türkiye)
- Recruiting
- Sağlık Bilimleri Üniversitesi
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Contact:
- sami eksert, MD, Assoc. Prof.
- Phone Number: +90 532 562 0597
- Email: exert79@yahoo.com
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study population consists of adult patients (18-99 years) scheduled for elective surgery under general anesthesia at a tertiary care hospital.
Participants represent typical surgical patients requiring preoperative airway assessment.
No healthy volunteers will be enrolled.
Only ASA I-III patients who can provide informed consent will be included.
Description
Inclusion Criteria:
- Adults aged 18-99 years
- Patients scheduled for elective surgery under general anesthesia
- ASA Physical Status I-III
- Able to provide informed consent
- Undergoing preoperative airway evaluation
Exclusion Criteria:
- - Emergency surgery cases
- Age <18 years
- ASA Physical Status IV-V
- Pregnant or breastfeeding patients
- Patients with limited cooperation or inability to provide consent
- Known anatomical airway anomalies or previous major neck surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Single Cohort
This cohort includes all adult participants undergoing airway evaluation with upper airway ultrasound and standard anthropometric measurements.
No interventions are applied; participants are observed prospectively to assess the predictive value of ultrasound parameters for difficult airway.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Diagnostic accuracy of ultrasound airway measurements for predicting difficult mask ventilation
Time Frame: Preoperative assessment (within 1 hour before induction of anesthesia)
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Evaluation of the sensitivity, specificity, and area under the ROC curve (AUC) of ultrasound-based airway measurements-tongue thickness, hyoid-to-skin distance, and epiglottis-to-skin distance-in predicting difficult mask ventilation.
These ultrasound parameters will be compared with conventional anthropometric airway assessment tests to determine their predictive performance.
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Preoperative assessment (within 1 hour before induction of anesthesia)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Yao W, Wang B. Can tongue thickness measured by ultrasonography predict difficult tracheal intubation? Br J Anaesth. 2017 Apr 1;118(4):601-609. doi: 10.1093/bja/aex051.
- Rastogi A, Singh AK, Srivastava D, Kannaujia AK, Singh TK, Mishra P. Evaluation of ultrasound measured tongue thickness, tongue thickness-thyromental distance ratio, and skin-to-epiglottis distance in predicting unanticipated difficult laryngoscopy. J Anaesthesiol Clin Pharmacol. 2025 Jan-Mar;41(1):151-157. doi: 10.4103/joacp.joacp_423_23. Epub 2025 Jan 23.
- Roth D, Pace NL, Lee A, Hovhannisyan K, Warenits AM, Arrich J, Herkner H. Airway physical examination tests for detection of difficult airway management in apparently normal adult patients. Cochrane Database Syst Rev. 2018 May 15;5(5):CD008874. doi: 10.1002/14651858.CD008874.pub2.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 25, 2025
Primary Completion (Estimated)
July 25, 2026
Study Completion (Estimated)
December 25, 2027
Study Registration Dates
First Submitted
December 16, 2025
First Submitted That Met QC Criteria
December 16, 2025
First Posted (Actual)
December 30, 2025
Study Record Updates
Last Update Posted (Actual)
March 10, 2026
Last Update Submitted That Met QC Criteria
March 6, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- AEŞH-EK-2-25-276
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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