Clinical Trials Directory

Trials / Completed

CompletedNCT00953433

Laryngeal Morbidity After Endotracheal Intubation - Endoflex-tube Versus Use of Stylet

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
130 (actual)
Sponsor
Rigshospitalet, Denmark · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is aimed at reducing the risk of hoarseness and damage to the vocal cords following general anaesthesia. Conventional endotracheal intubation with use of a stylet will be compared with the Endoflex tube. A conventional stylet enforced endotracheal tube is dirigible because of the stiffness gained by the addition of a stylet. In high risk rapid sequence intubation settings the enhanced dirigibility can be crucial, which is why most anaesthesiologists choose to add the stylet in these situations. A new endotracheal tube with a dynamic dirigible end called the Endoflex tube might prove to be a good alternative to the conventional stylet enforced endotracheal tube. Study hypothesis: The Endoflex tube will reduce the risk of hoarseness after intubation when compared to the conventional stylet enforced endotracheal tube under optimal intubation conditions.

Conditions

Interventions

TypeNameDescription
DEVICEEndoflex tubeSize decided upon gender.
DEVICEPolyvinyl chloride endotracheal tube with a styletSize decided upon gender.

Timeline

Start date
2010-04-01
Primary completion
2011-08-01
Completion
2011-08-01
First posted
2009-08-06
Last updated
2011-08-24

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00953433. Inclusion in this directory is not an endorsement.