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Clinical Trials/NCT02708420
NCT02708420
Completed
Not Applicable

Comparison of Hemodynamic Responses to Endotracheal Intubation With Glidescope Video Laryngoscope and Macintosh Direct Laryngoscope in Patients Undergoing Coronary Artery Bypass Surgery

Gata Haydarpasa Research Hospital1 site in 1 country70 target enrollmentJanuary 1, 2016
ConditionsBlood Pressure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Blood Pressure
Sponsor
Gata Haydarpasa Research Hospital
Enrollment
70
Locations
1
Primary Endpoint
Change in diastolic blood pressure
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Laryngoscopy and endotracheal intubation causes significant hemodynamic response and thus presents an increased risk for patients undergoing cardiac bypass surgery. Prevention or reduction of this increment is important for hemodynamic control. In this randomized single blind study, the aim of this study is to compare the hemodynamic responses of two different laryngoscopy techniques with Glidescope and Macintosh laryngoscope in coronary cardiac bypass surgery patients.

Detailed Description

Laryngoscopy and endotracheal intubation causes significant hemodynamic response and thus presents an increased risk for patients undergoing cardiac bypass surgery. Prevention or reduction of this increment is important for hemodynamic control. In this randomized single blind study, the aim of this study is to compare the hemodynamic responses of two different laryngoscopy techniques with Glidescope and Macintosh laryngoscope in coronary cardiac bypass surgery patients. After induction with our institutional protocol for cardiac bypass surgery, hemodynamic data including heart rate, systolic and diastolic arterial pressure data will be recorded. Time for intubation, age, sex, ASA status data will also be recorded.

Registry
clinicaltrials.gov
Start Date
January 1, 2016
End Date
June 1, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Gata Haydarpasa Research Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) physical Status 2-3
  • Patients undergoing elective cardiac bypass surgery

Exclusion Criteria

  • Difficult intubation history
  • Need for Rapid sequence intubation or alternative intubation method
  • Emergency procedures
  • Patients that have predictive factors for difficult intubation
  • Patients with permanent pacemaker

Outcomes

Primary Outcomes

Change in diastolic blood pressure

Time Frame: 5 minutes; At start of laryngoscopy and after 30th seconds, 60th seconds, 90th seconds, 120th seconds, 3rd minutes, 4th minutes, 5th minutes

invasive blood pressure (mmHg) monitoring

Change in mean arterial pressure

Time Frame: 5 minutes;At start of laryngoscopy and after 30th seconds, 60th seconds, 90th seconds, 120th seconds, 3rd minutes, 4th minutes, 5th minutes

invasive blood pressure (mmHg) monitoring

Change in heart rate

Time Frame: 5 minutes; At start of laryngoscopy and after 30th seconds, 60th seconds, 90th seconds, 120th seconds, 3rd minutes, 4th minutes, 5th minutes

Heart rate (beats per minute) will be measured before induction, and throughout and after laryngoscopy

Change in systolic blood pressure

Time Frame: 5 minutes; At start of laryngoscopy and after 30th seconds, 60th seconds, 90th seconds, 120th seconds, 3rd minutes, 4th minutes, 5th minutes

invasive blood pressure (mmHg) monitoring

Secondary Outcomes

  • Procedure time(10 minutes)
  • Cormack lehane laryngoscopic view will be recorded(10 minutes)

Study Sites (1)

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