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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02325076
Other study ID # 13-KAEK-215
Secondary ID
Status Completed
Phase N/A
First received December 11, 2014
Last updated February 10, 2016
Start date December 2013
Est. completion date February 2015

Study information

Verified date February 2016
Source Tokat Gaziosmanpasa University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Interventional

Clinical Trial Summary

The airflow moving from mouth to the lungs, which can be measured by pulmonary function tests, may be affected by the anatomic disorders of the upper airway. Difficult airway can be considered as the anatomic disorder of the upper airway as well. Therefore, there can be a relationship between difficult airway and pulmonary function tests. The purpose of this study is to elucidate the association between the pulmonary function tests and difficult airway.


Description:

After approval of the Gaziosmanpasa University Clinical Trials Ethics Committee, patients those admitted to the anesthesiology outpatient unit will informed about the study. And pulmonary function tests by using Spirodoc® will be performed to those willing to participate in the study. Measurements of the pulmonary function tests, and measurements belong to difficult airway will be recorded.

In the operating theatre, after induction of anesthesia, the difficult intubation measurements will be recorded.

Normality and variance will be tested using One Sample Kolmogorov-Smirnov test, skewness, kurtosis and histograms for each variable. Quantitative data will present as means and standard deviation, and qualitative data as frequency and percentage. Depending on these results, Spearman's correlation analysis will perform to show the association between pulmonary function tests and difficult airway measurements. Analyses were conducted using the Statistical Package for Social Sciences program (SPSS Inc., Chicago, IL), version 20.0. Statistical significance for all analyses was set at p < 0.05.


Recruitment information / eligibility

Status Completed
Enrollment 202
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Patients whose admitted to the Gaziosmanpasa University, Medical Faculty, Anesthesiology and Reanimation outpatient unit

- Patients whose will be planned to undertake a surgical operation under general anesthesia and those performed tracheal intubation to secure the airway.

- An American Society of Anesthesiologists score of 1 or 2

Exclusion Criteria:

- Patient whose planned to undertake a surgical operation in the departments of ear-nose-throat, cardiac and vascular surgery, plastic and reconstructive surgery

- Patients with a history of chronic obstructive lung diseases

- Patients with a history of surgery on the neck

- Patients with a history of mandibular surgery

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Device:
Spirodoc
A device to detect the physical condition of the lungs

Locations

Country Name City State
Turkey Gaziosmanpasa University Tokat

Sponsors (1)

Lead Sponsor Collaborator
Tokat Gaziosmanpasa University

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Leiter JC. Upper airway shape: Is it important in the pathogenesis of obstructive sleep apnea? Am J Respir Crit Care Med. 1996 Mar;153(3):894-8. Review. — View Citation

Tucker Woodson B. Structural effectiveness of pharyngeal sleep apnea surgery. Sleep Med Rev. 2008 Dec;12(6):463-79. doi: 10.1016/j.smrv.2008.07.010. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Pulmonary function test differences between Mallampati 3 and 4 patients eighteen months No
Secondary Cormack-Lehane grade Cormack-Lehane grade eighteen months No
Secondary Maximum mouth opening Maximum mouth opening eighteen months No
Secondary Percentage of glottic opening Percentage of glottic opening eighteen months No
Secondary Upper lip bite test score Upper lip bite test score eighteen months No
Secondary Measurement of neck circumference Measurement of neck circumference eighteen months No
Secondary Sterno-mental distance Sterno-mental distance eighteen months No
Secondary Thyromental distance Thyromental distance eighteen months No
Secondary Mean inspiratory flow eighteen months No
Secondary The ratio of forced expiratory flow 25% to forced expiratory flow 75% eighteen months No
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