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NCT04459481 Clinical Trial

Comparison of Two Bending Angles for Nasotracheal Intubation With a Malleable Vedio Stylet

Intubation;Difficult Clinical Trial

Official title:
Comparison of Two Bending Angles for Nasotracheal Intubation With a Malleable Vedio Stylet

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04459481
Other study ID # PSH-2018-13
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 4, 2020
Est. completion date November 5, 2020

Study information
Verified date January 2021
Source Chinese Academy of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Video intubating stylet can be safely and effectively used for nasotracheal intubation, but the optimal bending angle is still unknown. In this study, the optimal bending angle will be determined by comparing the intubation time and success rate of nasotracheal intubation with video intubating stylet at two different bending angles.

Description:

intubation will be accomplished at 70 bending angle and 90 degrees bending angle in each group. intubation time, success rate, additional manoeuvres and epistaxis will be recorded and compared.

Recruitment information / eligibility
Status Completed
Enrollment 98
Est. completion date November 5, 2020
Est. primary completion date November 3, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patients require nasotracheal intubation Exclusion Criteria: - fixed, or limited, neck movement, obstructive sleep apnoea, bilateral nasal obstruction or patients with an abnormal coagulation status

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• bending angle
patients in 70-degree bending angle group are intubated with video stylet at 70-degree bending angle patients in 90-degree bending angle group are intubated with video stylet at 90-degree bending angle

Locations
Country Name City State
China ChineseAMS Beijing Beijing

Sponsors (1)
Lead Sponsor Collaborator
Chinese Academy of Medical Sciences

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Success rate of nasotracheal intubation The percentage of successful nasotracheal intubation Procedure (From the beginning of intubation to the end of intubation)
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