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View Clinical Trial (Medical Research Study)


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

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City:   San Francisco
State:   California
Zip Code:   94143
Conditions:   Post Operative Sore Throat - Dysphagia - Hoarseness
Purpose:   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 Summary:  
Criteria:   Inclusion Criteria: - Scheduled for general anesthesia requiring endotracheal intubation with planned duration of at least 2 hours - ASA I-3 Exclusion Criteria: - Planned prolonged intubation - Planned postoperative ICU admission - Non English speaking - Mentally impaired - Existing tracheal stoma - Nasogastric tube in place preoperative - Thyroid / intra-oral surgery - Previous general anesthesia within the last 2 weeks - Use of steroids within one week before surgery (IV,inhaled, oral)
NCT ID:   NCT01305265
Primary Contact:   N/A
Backup Contact:   N/A
Location Contact:   San Francisco, California 94143
United States



There is no listed contact information for this specific location.

Site Status: N/A

Data Source:   ClinicalTrials.gov
Date Processed:   May 22, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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