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CompletedNCT01305265

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
141 (actual)
Sponsor
University of California, San Francisco · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEcuff manometerendotracheal tube cuff will be inflated to 22-26 cm H20 using cuff manometer

Timeline

Start date
2011-11-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2011-02-28
Last updated
2014-02-26
Results posted
2014-02-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01305265. Inclusion in this directory is not an endorsement.

Post-operative Sore Throat as Determined by Endotracheal Tube Inflation Technique (NCT01305265) · Clinical Trials Directory