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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02267759
Other study ID # AJIRB-DEV-DE1-14-312
Secondary ID
Status Completed
Phase N/A
First received October 14, 2014
Last updated June 17, 2015
Start date November 2014
Est. completion date March 2015

Study information

Verified date June 2015
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

McGrath videolaryngoscopy avoids the use of Magill forceps for nasotracheal intubation, thereby reducing intubation time and complications, especially in patients with a difficult airway. This study was performed to investigate whether McGrath videolaryngoscopy is superior to Macintosh laryngoscopy for routine nasotracheal intubation in expected normal airways, as judged by the time to intubation and ease of intubation.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date March 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- patients for dental or maxillofacial surgery requiring nasotracheal intubation

Exclusion Criteria:

- known difficult airway

- required rapid sequence induction

- history of bleeding

- cervical spine injury

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)


Related Conditions & MeSH terms


Intervention

Device:
McGrath videolaryngoscopy
After the softened nasotracheal tube was inserted into the nares until its tip passed through the posterior nares, McGrath videolaryngoscope was introduced into the mouth and the nasotracheal tube was advanced.
Macintosh laryngoscopy
After the softened nasotracheal tube was inserted into the nares until its tip passed through the posterior nares, Macintosh laryngoscope was introduced into the mouth and the nasotracheal tube was advanced.

Locations

Country Name City State
Korea, Republic of Ajou University Hospital Suwon Gyeongki-do

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 time to intubation time the nasotracheal tube was inserted into nares until endtidal CO2 was detected 4 min after anesthetic induction No
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