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NCT04503031 Clinical Trial

Comparison of Nasal Taper-guard Cuffed and a Nasal Cylindrical Endotracheal Tube

Endotracheal Tube Clinical Trial

Official title:
Comparison of the Endotracheal Tube Cuff Pressure Between a Taper-guard Cuffed Nasal Endotracheal Tube and a Cylindrical-shaped Cuffed Nasal Endotracheal Tube After Changing in Position of Head

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04503031
Other study ID # 2019-11-043-001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 10, 2020
Est. completion date August 1, 2020

Study information
Verified date October 2020
Source Kyungpook National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was designed to evaluate the effect of change of head position on the cuff pressure of TaperGaurd endotracheal tube , compared to cylindrical endotracheal tube during oral surgery.

Description:

The patient in cylindrical group (n=26) were intubated with cylindrical shaped endotracheal tube (Unomedical, Kedah, Malaysia) and the patient in tapergaurd group (n=26) was intubated with TaperGuard endotracheal tube (Covidien, Athlone, Ireland). The group allocations were informed to the attending anesthesiologist prior to anesthesia. Tracheal intubation was performed with size of inner diameter 7.0 mm endotracheal tube for male and 6.5 mm endotracheal tube for female by the same anesthesiologist. The anesthesiologist measured cuff pressure and distance from endotracheal tube tip to carina during study period.This study was designed to evaluate the effect of change of head position on the cuff pressure of TaperGaurd endotracheal tube, compared to cylindrical endotracheal tube during oral surgery.

Recruitment information / eligibility
Status Completed
Enrollment 52
Est. completion date August 1, 2020
Est. primary completion date August 1, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patient who were underwent nasal intubation Exclusion Criteria: - history of difficult intubation, limited neck movement, respiratory diseases and body mass index more than 35 kg/m2

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• TaperGuard endotracheal tube
TaperGuard endotracheal tube is intubated
• cylindrical endotracheal tube
endotracheal tube is intubated

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

Sponsors (1)
Lead Sponsor Collaborator
Kyungpook National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cuff pressure Cuff pressure is measured with a manometer (Mallinckrodt Medical, Hennef, Germany). 5 minutes after change of head position
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