We are assessing the effectiveness of high supply of oxygen when patient is not breathing during Fibre Optic Intubation under General Anaesthesia
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056194
- Lead Sponsor
- Dr. Bhavyashree. V
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient aged 18 - 65 years
Patients with Mallampati grade I and II
Patients belonging to American Society of Anaesthesiologists Physical Status (ASA-PS)I and II
Exclusion Criteria
Patients with history of stridor and or obstructive sleep apnea (OSA)
Patients with known airway pathology, DNS and morbid obesity
Pregnant and lactating mothers
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To observe the oxygen saturation during the Oral Fibreoptic Intubation following <br/ ><br>preoxygenation & apnoeic oxygenation with high flow nasal cannula.Timepoint: Perioperative, until patient is shifted from the recovery room
- Secondary Outcome Measures
Name Time Method To observe the oxygen saturation during the Oral Fibreoptic Intubation following <br/ ><br>preoxygenation & apnoeic oxygenation with high flow nasal cannula.Timepoint: After induction to larygoscopy & intubation;To observe the oxygen saturation during the Oral Fibreoptic Intubation following <br/ ><br>preoxygenation & apnoeic oxygenation with high flow nasal cannula.Timepoint: After induction to larygoscopy & intubation