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NCT03120546 Clinical Trial

Cervical Spine Motion During Tracheal Intubation: Video Laryngoscope vs Rigid Video Stylet

Intubation Clinical Trial

Official title:
A Randomized Comparison of Cervical Spine Motion During Tracheal Intubation Using Video Laryngoscope or Rigid Video Stylet in Patients With Simulated Cervical Immobilization

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03120546
Other study ID # McGrath vs Optiscope
Secondary ID
Status Completed
Phase N/A
First received April 14, 2017
Last updated February 12, 2018
Start date July 25, 2017
Est. completion date October 31, 2017

Study information
Verified date February 2018
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, investigators are going to compare cervical spine motion during tracheal intubation using video laryngoscope or rigid video stylet in patients with simulated cervical immobilization.

Description:

In patients with an unstable cervical spine, neck extension during tracheal intubation may result in harmful events such as spinal cord injury. Thus, it is important to minimize cervical spine motion in these patients. In this randomized crossover study, investigators are going to compare cervical spine motion during tracheal intubation using video laryngoscope or rigid video stylet in patients with simulated cervical immobilization.

Recruitment information / eligibility
Status Completed
Enrollment 22
Est. completion date October 31, 2017
Est. primary completion date October 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients aged 18-80 years undergoing elective endovascular cerebral aneurysm coiling to general anesthesia in a neuroangiography suite

Exclusion Criteria:

- Patients with upper airway abnormalities such as inflammation, abscesses, tumors, polyps, and trauma

- Patients with a medical history of gastroesophageal reflux disease and previous airway surgery, at high risk for aspiration, coagulation disorders, or a Hunt Hess grade of 3-5

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• rigid video stylet intubation
intubation using rigid video stylet
• video laryngoscope intubation
intubation using video laryngoscope

Locations
Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary maximum cervical spine motion maximum angles measured at the occiput-C1, C1-C2, C2-C5 segments during tracheal intubation
Secondary intubation time time interval between insertion of the device into the oral cavity and its removal during tracheal intubation
Secondary number of intubation trial number of intubation trial during tracheal intubation
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