Comparison of patient comfort during airway Ultrasound between Nasal versus Oral Route.
Not Applicable
- Conditions
- Health Condition 1: J985- Diseases of mediastinum, not elsewhere classifiedHealth Condition 2: C348- Malignant neoplasm of overlappingsites of bronchus and lungHealth Condition 3: A188- Tuberculosis of other specified organs
- Registration Number
- CTRI/2019/09/021298
- Lead Sponsor
- AIIMS Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients who have clear indication of EBUS procedure will be enrolled in the study.
2. Patients who give consent.
Exclusion Criteria
Patients who will not give consent and who have contraindications to Bronchoscopy / Endobronchial Ultrasound e.g. Uncooperative patient, refractory hypoxemia, unstable cardiaovascular status, facial deformity, recent/unstable angina, myocardial infarction within last 6 weeks, arrhythmias, bleeding disorders, uremia, etc will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To compare patient comfort during Endobronchial Ultrasound via nasal route and Oral routes. <br/ ><br>2.To compare failure rate of EBUS procedure in both the groups. <br/ ><br>Timepoint: During, after intubation and after 2 hours of procedure
- Secondary Outcome Measures
Name Time Method 1.To assess operator satisfaction (VAS) between the two groups. <br/ ><br>2.To assess willingness to return for the procedure. <br/ ><br>3.Comparison of NAPCOM scores. <br/ ><br>4.Comparison of cough count between the two procedure.(VAS) <br/ ><br>5.Comparison of Overall duration to reach in sub-glottic area. <br/ ><br>6.To compare mean dose of topical anaesthetic requirement. <br/ ><br>7.To measure difference of intravenous analgesic/ sedative requirement between the two groups <br/ ><br>8.To compare complications rate between two groups. <br/ ><br>Timepoint: During, after intubation and after 2 hours of procedure