Comparison of the Cuff Pressure of TaperGuard and Cylindrical- Endotracheal Tube During Laparoscopic Surgery

Cuff Pressure Clinical Trial

Official title:

Comparison of the Cuff Pressure of TaperGuard Endotracheal Tube and Cylindrical- Endotracheal Tube During Laparoscopic Surgery

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03040440
• Other study ID #: KNUH 2016-03-001-004
• Status: Completed
• Phase: N/A
• First received: January 31, 2017
• Last updated: January 31, 2017
• Start date: June 1, 2016
• Est. completion date: December 30, 2016

Study information

• Verified date: January 2017
• Source: Kyungpook National University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study was to compare the cuff pressure between cylindrical and TaperGuard endotracheal tube during laparoscopic cholecystectomy.

Description:

Sixty four participants were assigned to one of the two groups: cylindrical and TaperGuard endotracheal tube. At the supine position, cuff pressure of endotracheal tube was measured before and after abdominal insufflation in the supine position. After insufflation the head-up position (30°) was made and cuff pressure was recorded.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 64
• Est. completion date: December 30, 2016
• Est. primary completion date: December 15, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Participants who were underwent laparoscopic cholecystectomy with American Society of Anesthesiologists physical status 1-3

Exclusion Criteria:

• history with respiratory disease, difficult intubation, and morbid obesity (body mass index more than 35 kg/m2).

Related Conditions & MeSH terms

• Cuff Pressure

Intervention

Device:
• Cylindrical endotracheal tube
Cylindrical endotracheal tube was intubated
• TaperGaurd endotracheal tube
TaperGaurd endotracheal tube was intubated

Locations

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

Sponsors (1)

Lead Sponsor	Collaborator
Kyungpook National University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	cuff pressure		5 minutes after intubation