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NCT03582787 Clinical Trial

A Comparison of McGrath MAC Videolaryngoscopy and Macintosh Laryngoscopy for Orotracheal Intubation in Children With Torticollis

Anesthesia, Endotracheal Clinical Trial

Official title:
Ajou University School of Medicine

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03582787
Other study ID # AJIRB-MED-OBS-18-106
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 31, 2018
Est. completion date May 25, 2019

Study information
Verified date July 2019
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary purpose of this study is to investigate the effects of McGrath MAC videolaryngoscopy on the intubation time for orotracheal intubation in children with torticollis.

The secondary purpose of this study is to investigate the effects of McGrath MAC videolaryngoscopy on Cormack and Lehane Grade for orotracheal intubation in children with torticollis.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date May 25, 2019
Est. primary completion date May 25, 2019
Accepts healthy volunteers No
Gender All
Age group 1 Year to 10 Years
Eligibility Inclusion Criteria:

- orotracheal intubation under general anesthesia

- torticollis

Exclusion Criteria:

- •oral lesions, congenital anomaly, cervical spine instability, rapid sequence intubation

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• McGrath MAC videolaryngoscopy
Orotracheal intubation with McGrath MAC videolaryngoscopy after anesthetic induction
• Macintosh Laryngoscopy
Orotracheal intubation with Macintosh Laryngoscopy after anesthetic induction

Locations
Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Ajou University School of Medicine Suwon Seoum

Sponsors (1)
Lead Sponsor Collaborator
Ajou University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intubation time Time interval between laryngoscopy passing the teeth to the confirming of end tidal CO2 through intubation completion, an average of 30 second
Secondary The degree of glottic exposure as assessed by Cormack and Lehane Grade Grade 1: full view of glottis, grade 2: Partial view of glottis, grade 3:only epiglottis seen, grade 4:neither glottis nor epiglottis seen Up to 5 second after laryngoscopy passing the teeth
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