Viewing Study NCT04503031



Ignite Creation Date: 2024-05-06 @ 3:02 PM
Last Modification Date: 2024-10-26 @ 1:41 PM
Study NCT ID: NCT04503031
Status: COMPLETED
Last Update Posted: 2020-10-28
First Post: 2020-08-03

Brief Title: Comparison of Nasal Taper-guard Cuffed and a Nasal Cylindrical Endotracheal Tube
Sponsor: Kyungpook National University Hospital
Organization: Kyungpook National University Hospital

Study Overview

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
Status: COMPLETED
Status Verified Date: 2020-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: The patient in cylindrical group n26 were intubated with cylindrical shaped endotracheal tube Unomedical Kedah Malaysia and the patient in tapergaurd group n26 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 70 mm endotracheal tube for male and 65 mm endotracheal tube for female by the same anesthesiologist The anesthesiologist measured cuff pressure and distance from endotracheal tube tip to carina during study periodThis 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None