- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05673707
The Effect of Thyromental Height and Other Difficult Airway Evaluation Parameters
December 21, 2022 updated by: Savas Altinsoy, Diskapi Yildirim Beyazit Education and Research Hospital
The Effect of Thyromental Height and Other Difficult Airway Evaluation Parameters on Laryngeal Mask Placement Success Rate in Elderly Patients
Many changes occur in the body with age.
There are difficulties in endotracheal intubation and the placement of supraglottic airway devices (LMA) in elderly patients due to changes in the tooth and facial structure, and a decrease in temporomandibular joint and neck movements.
In the literature, there are studies on the relationship between thyromental height measurement and endotracheal intubation difficulty, but there is no study on the relationship between thyromental height measurement and laryngeal mask placement difficulty.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Age, gender, height, body weight, body mass index, type of operation, and Mallampati score are recorded in the preoperative evaluations of all patients.
For anthropometric measurements, thyromental height, thyromental distance, sterno-mental distance, neck circumference, and mouth opening are measured.
After the laryngeal mask is placed after the induction of anesthesia, the location of the LMA is checked with the FOB (fiberoptic bronchoscopy).
Ease of insertion was subjectively assessed using a grading score of 1-4 (1, no resistance; 2, mild resistance; 3, moderate resistance; 4, inability to insert the device) by the attending anesthesiologist who inserted the device.
After successful placement of the device, the adjustable pressure limiting (APL) valve is adjusted to 30 cm H2O at 3L/minute fresh gas flow, and the airway pressure and leakage amount are measured.
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: savaş altınsoy
- Phone Number: +903125962523
- Email: savasaltinsoy@gmail.com
Study Locations
-
-
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Ankara, Turkey, 06450
- Recruiting
- Department of Anesthesiology and Reanimation, University of Health Sciences, Diskapi Yıldırım Beyazit Training and Research Hospital
-
Contact:
- savaş altınsoy
- Phone Number: +903125962523
- Email: savasaltinsoy@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years to 90 years (Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
all patients between 65-90 years old who had urological procedure
Description
Inclusion Criteria:
- over 65 years old
- elective operation
- using laryngeal mask device
Exclusion Criteria:
- younger than 65 years old
- urgent or emergency operation
- morbidity obese
- contraindications of all laryngeal mask devices using
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
laryngeal mask placement success
Time Frame: during insertion
|
The correlation between preoperative thyromental height measurement and laryngeal mask placement success
|
during insertion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2022
Primary Completion (Actual)
July 30, 2022
Study Completion (Anticipated)
January 30, 2023
Study Registration Dates
First Submitted
December 21, 2022
First Submitted That Met QC Criteria
December 21, 2022
First Posted (Estimate)
January 6, 2023
Study Record Updates
Last Update Posted (Estimate)
January 6, 2023
Last Update Submitted That Met QC Criteria
December 21, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- LMA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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