Clinical Trials Directory

Trials / Completed

CompletedNCT03385044

Comparison of Endotracheal Intracuff Pressure Between Two Cuff Sealing Methods

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
35 (actual)
Sponsor
DongGuk University · Academic / Other
Sex
Female
Age
20 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The endotracheal intracuff pressure is to be maintained at a low level to prevent trachea and nerve damages, and yet be high enough to secure air sealing. The objective of the study is to compare minimal occlusive volume technique (MOVT) and expired volume/inspired volume ratio (VE/VI ratio) from a spirometer method of endotracheal tube (ETT) cuff inflation with respect to the cuff pressure required to seal the airway during a laparoscopic surgery under general anesthesia. A study design is a randomized crossover trial in 35 patients. The primary outcome is the intracuff pressure of an endotracheal tube. The study consists of two cuff sealing methods separated by a period of 10 minutes.

Conditions

Interventions

TypeNameDescription
PROCEDUREMOVTETT cuff will be inflated till the disappearance of audible air leak on auscultation, while abdominal carbon dioxide (CO2) inflation is maintained with peak inspiratory pressure of 25 cm H2O during volume controlled ventilation. The patient will be in the Trendelenburg position.
PROCEDUREVE/VI ratio of SpirometerETT cuff will be inflated till the VE/VI ratio meets the initial VE/VI ratio, while abdominal CO2 inflation is maintained with peak inspiratory pressure of 25 cm H2O during volume controlled ventilation. The patient will be in the Trendelenburg position.

Timeline

Start date
2018-03-12
Primary completion
2018-10-29
Completion
2018-10-29
First posted
2017-12-28
Last updated
2018-12-14

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03385044. Inclusion in this directory is not an endorsement.