comparing intubation in trachea with two devices in patients with snoring who are risk for difficult intubation using an assessing score
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061055
- Lead Sponsor
- Hamadard Institute of Medical Sciences and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American society of anesthesiologist grade I-II , Morbidly obese patients, Age >18, Stop bang scoring >3 posted for elective surgery under General Anaesthesia
Exclusion Criteria
1. Patient refusal to give consent
2. Patient with laryngeal or pharyngeal pathology
3. Patient mouth opening <20mm
4. Lean body < 50kg
5. Pregnant patients
6. Patient with Heart rate <60
7. Patient with local anaesthetic allergy
8. Patient with airway bleeding
9. Patient with fixed flexion deformity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare time to intubation using flexible bronchoscope and video-laryngoscope for awake oral tracheal intubation in patients at risk of OSA.Timepoint: Total time for for intubation
- Secondary Outcome Measures
Name Time Method 1. To compare first attempt success rate between the groups <br/ ><br>2. To compare hemodynamic response to intubation between the groups <br/ ><br>3. To compare patient discomfort score between the groups <br/ ><br>4. To compare intraoperative complications like episodes of desaturation ( <93%) and <br/ ><br>oropharyngeal mucosal damageTimepoint: Hemodynamic response over 15 minutes after intubation <br/ ><br>Monitor post-operative complication over 24 hours