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

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

      • Ankara, Turkey (Türkiye)
        • Recruiting
        • Sağlık Bilimleri Üniversitesi
        • Contact:
          • sami eksert, MD, Assoc. Prof.
          • Phone Number: +90 532 562 0597
          • Email: exert79@yahoo.com

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
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diagnostic accuracy of ultrasound airway measurements for predicting difficult mask ventilation
Time Frame: Preoperative assessment (within 1 hour before induction of anesthesia)
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.
Preoperative assessment (within 1 hour before induction of anesthesia)

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.

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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