Actively Recruiting
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
Eligibility Criteria
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
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
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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