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Post-operative Sore Throat as Determined by Endotracheal Tube Inflation Technique

Dysphagia Clinical Trial

Official title:
Post-operative Sore Throat as Determines by Endotracheal Tube Inflation Technique

Clinical Trial Summary

The purpose of this study is to test whether the incidence of sore throat and other tracheal co-morbidities such as dysphagia and hoarseness can be lessened by use of a cuff manometer at the beginning of surgery to inflate to the proper pressure compared to the standard technique.

The investigators hypothesis is that inflation of the endotracheal balloon using a cuff manometer immediately after intubation will reduce the incidence of sore throat and other tracheal co-morbidities.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01305265
Study type Interventional
Source University of California, San Francisco
Contact
Status Completed
Phase N/A
Start date November 2011
Completion date December 2012
View Details
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