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Comparison of Ultrasonographic and Anthropometric Measurements in Difficult Airway Evaluation

Completed
Conditions
Difficult Airway Intubation
Interventions
Device: ultrasounography
Registration Number
NCT04140981
Lead Sponsor
Kırıkkale University
Brief Summary

In this study, anthropometric measurements (clinical measurements) will be applied in all patient groups; expected (to be difficult to provide airway patency as a result of detailed history, physical examination and evaluation tests performed by an experienced anesthesiologist), and unexpected (although it was not predicted that a difficulty was encountered). And ultrasounographic measurements will be applied in all patients. The aim of this study is to evaluate the predictive accuracy of ultrasonographic measurements.

Detailed Description

In the preoperative period, the following clinical tests will be performed before the patient arrives in the operating room and when the patient arrives, the measurements will be made by ultrasonography.

1. Mallampati classification

2. Determination of mouth opening (interinsizer distance)

3. Thyromental distance

4. Sternomental distance

Preoperative evaluation of the patients and clinical results of the airway tests (mentioned above) will be recorded. The cervical soft tissue thickness will be measured and recorded at 3 levels (thyrohyoid membrane, vocal cord, hyoid bone) with the help of ultrasonography (mentioned above). In addition, since all patients will be under general anesthesia, laryngoscopic images (laryngoscopic evaluation according to Cormack Lehane classification) routinely recorded on the anesthesia follow-up sheet will be recorded.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
127
Inclusion Criteria
  • patients under general anesthesia
  • ASA 1-2-3
Exclusion Criteria
  • Patients who will undergo emergency surgery,
  • pregnant women,
  • children,
  • patients who may have difficulty in airway management due to cervical instability,
  • patients with trauma or malignancy in the neck region

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
group 1ultrasounographydifficult intubation according to antropometric measurements
group 2ultrasounographynot difficult intubation according to antropometric measurements
group 3ultrasounographydifficult intubation according to ultrasound measurements
group 4ultrasounographynot difficult intubation according to ultrasound measurements
Primary Outcome Measures
NameTimeMethod
Cormack Lehane classificationduring the intubation period

Laryngoscopic evaluation according to Cormack Lehane classification

Secondary Outcome Measures
NameTimeMethod
ultrasonographic measurement15 min before the operation

Preoperative ultrasonographic measurement will be made

Trial Locations

Locations (1)

Kırıkkale Univercity Faculty of Medicine Hospital

🇹🇷

Kırıkkale, Turkey

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