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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03759990
Other study ID # KOU-KAEK 2018 - 202
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date December 1, 2018

Study information

Verified date March 2020
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

80 lean (BMI<35) and morbidly obese (BMI>35) patients undergoing elective surgery were enrolled in this prospective ransomÄ°zed study were intubated using McGrath MAC X-Blade. The demographic and airway variables of patients and insertion and intubation times with these dievices, need for optimisation maneuvers, hemodynamic changes and minör postoperative complications were recorded.


Description:

80 lean (BMI<35) and morbidly obese (BMI>35) patients undergoing elective surgery were enrolled in this prospective ransomÄ°zed study were intubated using McGrath MAC X-Blade. The demographic and airway variables of patients were recorded. Airway management variables Cormack-Lehan grades, insertion and intubation times, need for optimization maneuvers ( cricoid pressure, re-inserting, drawback) , hemodynamic changes in heart rate , blood pressure and minor postoperative complications such as sore throat, dysphasia, hoarseness were recorded.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 1, 2018
Est. primary completion date December 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: > 18 age <65 age

- bmi 35

- undergoing elective surgery requiring endotracheal intubation

Exclusion Criteria: -pregnant

- <18 and >65 years of age

- bmi<35

- upper respiratory tract infection past ten days

Study Design


Related Conditions & MeSH terms


Intervention

Device:
lean
Videolaryngoscope used in intubation
obese
Videolaryngoscope used in intubation

Locations

Country Name City State
Turkey Kocaeli University Medical Faculty Kocaeli
Turkey Kocaeli University School of Medicine Kocaeli

Sponsors (1)

Lead Sponsor Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary intubation time 2 months
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