NCT07528677Not yet recruiting
Ultrasound vs Clinical Parameters for Difficult Airway Prediction in Obesity
Comparison of Airway Ultrasonography and Conventional Difficult Airway Parameters for Predicting Difficult Airway in Obese Patients: A Prospective Observational Study
Source: ClinicalTrials.gov · Last updated 14 Apr 2026
Brief summary (registry, in English)
Obesity is associated with anatomical changes in the upper airway that increase the risk of difficult laryngoscopy and difficult mask ventilation during anesthesia. Conventional airway assessment parameters such as Mallampati score, neck circumference, and STOP-BANG scale are widely used but have limited predictive accuracy in obese patients. Airway ultrasonography has emerged as a promising non-invasive tool for difficult airway prediction; however, ultrasonographic criteria have not yet been standardized. This prospective observational study aims to evaluate the utility of airway ultrasonography in predicting difficult airway in adult obese patients (BMI \>30 kg/m²) scheduled for elective surgery under general anesthesia. Ultrasonographic measurements will include the distance from skin to hyoid bone (DSHB) at the level of the hyoid bone, the anterior neck soft tissue thickness at the thyrohyoid membrane level, and the hyomental distance ratio (HMDR). These parameters will be compared with conventional airway assessment tools and correlated with intraoperative Cormack-Lehane laryngoscopy grade and Han Scale mask ventilation score to determine their predictive value for difficult airway.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 70 (estimated)
- First submitted
- 27 Mar 2026
- Start date
- 10 Apr 2026
- Primary completion date
- 10 Oct 2026
- Lead sponsor
- Fatih Sultan Mehmet Training and Research Hospital
- Diseases
- Obesity
- NCT number
- NCT07528677
What you commit to
- Study type: Observational
- Planned participants: 70
- From 10 Apr 2026 to the primary completion date, 10 Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Emergency surgery
- History of previous head and neck surgery or radiotherapy
Other illness
- Known or anticipated difficult airway (history of difficult intubation)
Other
- Presence of cervical spine pathology or limited neck mobility
- Presence of oropharyngeal or laryngeal pathology
- Pregnancy
- Patients with tracheostomy
- Refusal to participate
Who the study is looking for
- Age 18-65 years
- BMI \>30 kg/m2
- ASA physical status I, II, or III
- Scheduled for elective surgery requiring orotracheal intubation under general anesthesia
- Written informed consent obtained
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Fatih Sultan Mehmet Training and Research Hospital Coordinator of this site? Confirm its status | Istanbul | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.