Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07482436

Comparison of Airway Ultrasonography and Laryngoscopy Methods in Obese Patients

Led by Trabzon Kanuni Education and Research Hospital · Updated on 2026-03-19

180

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main objective of this study was to examine the relationship between classical markers used in assessing difficult airway management in obese patients (Mallampati score, thyromental distance, sternomental distance, neck circumference measurement) and ultrasonographic parameters (vocal cord mobility, glottic opening, hyomental distance, skin-epiglottic distance, and peri-epiglottic space-epiglottic-vocal cord ratio), to compare the effects of these parameters on predicting difficult intubation, and to investigate the effects of different laryngoscopy methods on intubation success and peroperative respiratory complications. The secondary objective of the study is to investigate the effects of different laryngoscopy methods on hemodynamic responses to intubation. Participants' gender, age, height, weight, BMI, ASA physical status classification, smoking status, comorbidities, STOP-BANG and LEMON scores will be recorded. The glottic score percentage (POGO score), glottic visualization time, endotracheal intubation time, use of assistive maneuvers, and Intubation Difficulty Scale (IDS) parameters will be compared according to the laryngoscopy methods used. Participants must meet the following criteria: * Consent given by the patient * Operated under general anesthesia * Over 18 years of age * American Society of Anesthesiologists (ASA) physical status classification I-II-III * Body mass index (BMI) of 30 kg/m2 or higher * Operation duration between 60-150 minutes * Patients undergoing elective surgery.

CONDITIONS

Official Title

Comparison of Airway Ultrasonography and Laryngoscopy Methods in Obese Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient consent given
  • Undergoing surgery with general anesthesia
  • Age 18 years or older
  • ASA physical status I, II, or III
  • Body mass index (BMI) 30 kg/m2 or higher
  • Surgery duration between 60 and 150 minutes
  • Elective surgery planned
Not Eligible

You will not qualify if you...

  • No patient consent
  • Undergoing head and neck surgery
  • Surgery performed in prone position
  • Uncooperative or unable to communicate
  • Presence of craniofacial anomalies
  • Emergency surgery planned

AI-Screening

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Trial Site Locations

Total: 1 location

1

Trabzon University Faculty of Medicine Kanuni Training and Research Hospital

Trabzon, Turkey (Türkiye), 61040

Actively Recruiting

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Research Team

E

Ezgi Günaydın, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

3

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