Clinical Trials Directory

Trials / Completed

CompletedNCT02294422

Balloon Palpation vs Loss of Resistance Syringe for Safe Endotracheal Tube Cuff Pressure; a Randomized Clinical Trial

Achieving Recommended Endotracheal Tube Cuff Pressure; A Randomized Control Trial Comparing Loss of Resistance Syringe to Pilot Balloon Palpation.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
178 (actual)
Sponsor
Makerere University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is aimed at establishing whether use of loss of resistance syringe (LOR) that is traditionally used for identifying epidural space, is a better method for providing safe cuff pressures in adults intubated with cuffed endotracheal tubes. The conventional method is the use of pilot ballon palpation (PBP) to approximate cuff pressures but this is associated with airway damage. The study hypothesis states that both the loss of resistance syringe method and the pilot balloon palpation methods achieve the recommended endotracheal tube intracuff pressures.

Conditions

Interventions

TypeNameDescription
DEVICEPBPthe pilot balloon is continuously palpated o felt for adequate pressure as its being inflated.
DEVICELOR
DEVICEAneroid manometerThe pilot balloon is attached onto the manometer and cuff pressures are raed off from the gauge.

Timeline

Start date
2014-04-01
Primary completion
2015-02-01
Completion
2015-02-01
First posted
2014-11-19
Last updated
2015-06-30

Locations

1 site across 1 country: Uganda

Source: ClinicalTrials.gov record NCT02294422. Inclusion in this directory is not an endorsement.