Post-operative Sore Throat as Determined by Endotracheal Tube Inflation Technique
- Conditions
- HoarsenessDysphagiaPost Operative Sore Throat
- Registration Number
- NCT01305265
- Lead Sponsor
- University of California, San Francisco
- Brief 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.
- Detailed Description
- Not available 
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 141
- Scheduled for general anesthesia requiring endotracheal intubation with planned duration of at least 2 hours
- ASA I-3
- 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)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
- Name - Time - Method - Incidence of Tracheopharyngeal Symptoms - within 2 hours after extubation 
- Secondary Outcome Measures
- Name - Time - Method 
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (1)
- University of California San Francisco 🇺🇸- San Francisco, California, United States University of California San Francisco🇺🇸San Francisco, California, United States
