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NCT03483285 Clinical Trial

Comparison of Two Different Videolaryngoscopes Regarding Hemodynamic Parameters in Open Heart Surgey

Intubation;Difficult Clinical Trial

Official title:
Videolaryngoscopes in Open Heart Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03483285
Other study ID # KOU-KAEK 2017-405
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2018
Est. completion date March 21, 2019

Study information
Verified date February 2021
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Endotracheal intubation increased the heart rate and blood pressure in normal patients. Open heart surgery patients are more prone to hemodynamic variability. In addition, they have increased possibility for difficult intubation The heart rate and blood pressure increase impaired the oxygen consumption. This was previously shown that Videolaryngoscopes minimaly effects the vital signs in normal patients. Videolaryngoscopy inreased the rate of success in normal and difficult airway. This study aimed to compare two laryngoscopes regarding hemodynamic parameters and intubation times in coronary bypass surgery.

Description:

Aim: Endotracheal intubation increased the heart rate and blood pressure in normal patients. Open heart surgery patients are more prone to hemodynamic variability. In addition, they have increased possibility for difficult intubation The heart rate and blood pressure increase impaired the oxygen consumption. This was previously shown that Videolaryngoscopes minimaly effects the vital signs in normal patients. Videolaryngoscopy inreased the rate of success in normal and difficult airway. This study aimed to compare two laryngoscopes regarding hemodynamic parameters and intubation times in coronary bypass surgery. Material and methods: 50 patients undergoing coronary bypass surgery enrolled in this prospective.randomized study. Demogaphic variables and airway characteristics of patients were recorded. Glottic visulisation and intubation time were recorded. Systolic blood pressure, diastolic blood pressure, mean arterial pressure and heart rate were recorded 2 minutes intervals before intubation, after intubation during 10 minutes.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date March 21, 2019
Est. primary completion date March 20, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - patients undergoing open heart surgery - < 18 years of age Exclusion Criteria: - emergency

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• airtraq
airtraq videolaryngoscope
• storz
storz videolaryngoscope

Locations
Country Name City State
Turkey Kocaeli University Hospital Kocaeli

Sponsors (1)
Lead Sponsor Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary heart rate heart rate 2 months
Secondary insertion time optimal glottic visualisation time 2 months
Secondary intubation time intubation time 2 months
Secondary mean arterial pressure mean arterial pressure 2 months
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