CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 141 enrolled
Drug / intervention
cuff manometerdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01305265
NCT01305265N/ACompleted

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

University of California, San Francisco·interventional·Posted Feb 28, 2011·Updated Feb 26, 2014

In Brief

A clinical study evaluating cuff manometer for Post Operative Sore Throat and 2 related conditions. Completed, enrolled 141 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 28, 2011
Enrollment StartNov 1, 2011
Primary CompletionDec 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 15.3 years ago

Interventions

cuff manometerdevice

endotracheal tube cuff will be inflated to 22-26 cm H20 using cuff manometer