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Face Index as Predictor of Difficult Airway and Intubation

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Study Aim

This study aims to observe and determine if certain facial features can predict difficulties in airway management and intubation procedures.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: March 2026
See protocol details

Summary

Principal SponsorOrdu University
Study ContactYasir İlyas, Ass. Prof.More contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: March 1, 2026

Actual date on which the first participant was enrolled.

This study focuses on patient safety during anesthesia, specifically on maintaining proper breathing. When a person is under anesthesia, their airway must be secured to ensure they can breathe properly. While simple face masks can often do the job, in some cases, a more reliable method called endotracheal intubation is needed. This involves inserting a tube into the windpipe to help with breathing. Certain physical characteristics, like facial structure, obesity, or a short neck, can make this process challenging. The study aims to introduce a new way of predicting these difficulties by using a measurement called the 'face index'. This could potentially simplify the prediction process, using a single value instead of multiple measurements. The study will compare traditional methods of predicting airway difficulties with the face index. This includes measurements like thyromental distance, neck circumference, and the Mallampati classification, among others. The face index involves measurements like the length from the hairline to the chin, total facial index, upper facial index, and nasal index. The study will investigate how well these measurements can predict difficulties at various stages of airway management, from using a face mask to inserting the endotracheal tube. All measurements used in this study are standard, non-invasive, and harmless, and are typically used by anesthesiologists as part of preoperative assessments.

Official TitleCan the "Face Index"; an Anthropometric Measurement, Predict Difficult Laryngoscopy and Intubation?
Principal SponsorOrdu University
Study ContactYasir İlyas, Ass. Prof.More contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1000 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: All adult patients over the age of 18 who have given written consent to undergo elective and/or emergency surgery under general anesthesia and be intubated in the operating rooms of our hospital's main building and annex building Exclusion Criteria: Patients with a prior history of difficult airway/difficult intubation, those who have undergone facial, neck, or airway surgery, those with deformities or scars in the facial and neck area due to burns or injuries, those with previous or recent tracheostomy, those with facial deformities due to any cause (congenital or acquired pathologies), and those with communication problems and who are uncooperative during measurements will be excluded from the study. Children and pregnant patients will not be included.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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