Observational study of THRIVE versus Conventional nasal oxygenation for apneic oxygenation in short bronchoscopy procedures
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: 4- Measurement and Monitoring
- Registration Number
- CTRI/2021/09/036344
- Lead Sponsor
- Dr Dixita Shetty
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I & II
Patients undergoing bronchoscopy procedures under general anaesthesia with LTS grade I, II, III (no respiratory distress)
Exclusion Criteria
Patients not willing to give consent
Patients with chronic respiratory disease (COPD)
Children with congenital airway anamolies, nasal bone#, DNS
BMI more than 30 kg/m2
Patients with room air saturation less than 98%
Pregnant & lactating mothers
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the effectiveness of THRIVE during apneic oxygenation for short bronchoscopy procedures and comparing it with nasal oxygenation supplementation method.Timepoint: At the time of procedure
- Secondary Outcome Measures
Name Time Method 1) To compare end tidal co2 changes <br/ ><br>2) To compare perioperative hemodynamic changes <br/ ><br>3) To note down complications if any.Timepoint: Intra operative and postoperative period