A prospective, single-blind, randomized clinical trial to evaluate the effectiveness of a new design of endotracheal suction catheter in reducing mucosal damage
Not Applicable
Recruiting
- Conditions
- Tracheal suction catheter
- Registration Number
- JPRN-UMIN000053145
- Lead Sponsor
- Seoul National University Bundang Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
- American Society of Anesthesiologists class > III - Patients taking antiplatelet and/or anticoagulation drugs - Patients who have abnormal coagulation lab (e.g. INR, PT, aPTT, platelet count) - Patients who have active respiratory infection (e.g. pneumonia)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tracheal injury grade
- Secondary Outcome Measures
Name Time Method - the number of endotracheal suction - vital signs before and after endotracheal suction (mean blood pressure, heart rate, SpO2) - the occurrence of bloody secretion when endotracheal suction is done - the satisfaction score about the function of endotracheal suction catheter (numerical rating scale from 0 to 10; 0-very unsatisfied, 10-very satisfied) - the score of sore throat during 24 hours after surgery (numerical rating scale from 0 to 10; 0-no pain, 10-pain to death) - the dose of opioid use during 24 hours after surgery - Other respiratory complications (e.g. hemoptysis, increase of secretion)