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Clinical Trials/NCT04140981
NCT04140981
Completed
Not Applicable

Evaluation of Ultrasounographic Measurements and Anthropometric Measurements as Predictors of Difficult Direct Laryngoscopy

Kırıkkale University1 site in 1 country127 target enrollmentOctober 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Difficult Airway Intubation
Sponsor
Kırıkkale University
Enrollment
127
Locations
1
Primary Endpoint
Cormack Lehane classification
Status
Completed
Last Updated
6 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 1, 2019
End Date
December 1, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Kırıkkale University
Responsible Party
Principal Investigator
Principal Investigator

Kevser Peker

assitant professor

Kırıkkale University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Cormack Lehane classification

Time Frame: during the intubation period

Laryngoscopic evaluation according to Cormack Lehane classification

Secondary Outcomes

  • ultrasonographic measurement(15 min before the operation)

Study Sites (1)

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