CClinicalTrials.gg
Not yet recruitingNCT07057661Updated Aug 20, 2025

Evaluation of Difficult Airway With Ultrasound

An observational study in Adenotonsillectomy Surgery, sponsored by Izmir City Hospital. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 3 Years to 8 Years. Per ClinicalTrials.gov, last updated 2025-08-20.

Sponsored by Izmir City Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Oct 2025, 11 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
3 Years to 8 Years
Sex
All
01

Study summary

An unexpected difficult airway can lead to severe hypoxia and even death. Accurate airway assessment can reduce the incidence of difficult endotracheal intubation and related complications. Studies have shown that some ultrasonic indicators can predict difficult airways in adults to some extent. Studies have begun to investigate whether ultrasonic parameters can be used to predict difficult airways in children.Ultrasonic measurements of certain airway parameters have predictive value for difficult airways; therefore, airway ultrasonography is recommended as an aid in difficult airway prediction. We think that in pediatric patients with adenotonsillectomy, we will encounter more difficult airway because there may be anatomical differentiation due to adenoid and tonsillar hypertrophy. We aimed to evaluate the frequency of difficult airway with USG measurements in pediatric patients undergoing adenotonsillectomy.

Group 1:Pediatric patients who underwent adenotonsillectomy Group 2: Pediatric patients who underwent any surgical operation We will evaluate two patient groups.

Read the detailed description

Ultrasonography (USG) is widely used in airway management, such as prediction of difficult airways, localization of cricothyroid membranes, selection of tracheal tubes, and evaluation of patients with a full stomach. Among these, ultrasonic measurements of the dimensions of certain airway parameters have predictive value for difficult airways; therefore, airway ultrasonography is recommended as an aid in difficult airway prediction. Many studies have shown that some ultrasonic parameters such as hyomental distance in the extension position and distance from the skin to the epiglottis can predict difficult airways in adults. However, it is unclear whether these parameters can be used to predict difficult airways in children. In recent studies, various protocols have started to be established . We think that we will encounter more difficult airways in pediatric patients with adenotonsillectomy because there may be anatomical differentiation due to adenoid and tonsillar hypertrophy. Therefore, we will evaluate the relationship between skin-epiglottic distance, hyomental distance and tongue base thickness measurements, which are used in most studies, and the mallampati score on physical examination and the Cormack Lehane score during laryngoscopy. The aim of this study was to compare the frequency of difficult airway between pediatric patients who underwent adenotonsillectomy (Group 1) and pediatric patients who underwent any surgical operation (Group 2) using USG measurements.

Group 1:Pediatric patients who underwent adenotonsillectomy Group 2: Pediatric patients who underwent any surgical operation

02

Conditions studied

  • Adenotonsillectomy Surgery

Keywords

  • airway management
  • pediatric patients
  • ultrasonography
03

In context

Lead sponsor

Izmir City Hospital is the lead sponsor of 23 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 8 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Pediatric patients who underwent adenotonsillectomy and any surgical operation

Inclusion criteria

  1. ASA 1-2 patients
  2. Pediatric patients aged 3-8
  3. Those planned for elective surgery

Exclusion criteria

Exclusion Criteria:

  1. Those with a history of congenital anomalies (head, face, body)
  2. ASA 3-4-5 patients
  3. Those who will undergo emergency surgery
  4. Those who will be subjected to an airway or anesthesia technique other than orotracheal intubation
  5. Newborn group patients
  6. Patients younger than 3 years old and older than 8 years old
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (estimated)
Patient registry
No

Groups and cohorts

  • Group 1: Pediatric patients who underwent adenotonsillectomy
  • Group 2: Pediatric patients who underwent any surgical operation
06

What researchers measure

Primary outcomes

  1. DSE: Distance from skin to epiglottis

    the vertical distances from the submental skin to the midpoint of the epiglottis

    Time frame: Preoperative , before the administration of anesthesia

  2. HMDE: Hyomental distance in the extended position

    the distance from the lower border of the mentum of the mandible to the upper border of the hyoid bone

    Time frame: Preoperative , before the administration of anesthesia

  3. Tongue base thickness

    Time frame: Preoperative , before the administration of anesthesia

Secondary outcomes

  1. Cormark Lehane score

    Grade 1: being a full view of the glottis Grade 2 : being a partial view Grade 3: being only a view of the epiglottis Grade 4: being an absent view of the glottis and epiglottis

    Time frame: During laryngoscopy

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07057661
Lead sponsor
Izmir City Hospital
Responsible party
Tuba Kuvvet Yoldaş (MD, Anesthesia Specialist, Izmir City Hospital) — Principal investigator
First posted
Jul 10, 2025
Start date
Aug 30, 2025 (estimated)
Primary completion
Oct 30, 2025 (estimated)
Completion
Nov 30, 2025 (estimated)
Last update
Aug 20, 2025

Study contacts

Tuba Kuvvet Yoldas, MD
Contact
tubayoldas2297@gmail.com
+905053428504
Tuba Kuvvet Yoldas, MD, Anesthesiology Specialist
principal investigator · Izmir City Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion