Clinical study for comparison of two new Video-Laryngoscopes in adult patients.
Not Applicable
Completed
- Conditions
- Health Condition 1: T07- Unspecified multiple injuries
- Registration Number
- CTRI/2020/09/027899
- Lead Sponsor
- Department of Anesthesiology and Critical Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 74
Inclusion Criteria
All patients with ASA physical status I or II of either sex, aged between 20 and 60 years and BMI 20-35kg/m2, presenting for elective surgery under General Anesthesia will be included in the study.
Exclusion Criteria
1. Potential risk of regurgitation (like GERD)
2. Pregnancy
3. Patients with an anticipated difficult airway (MPG III and IV and mouth opening less than 2 Finger-breadth)
4. Suspected cervical spine injury and neck instability
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method First attempt success rate of intubationTimepoint: At baseline
- Secondary Outcome Measures
Name Time Method 1. Time to visualize glottis <br/ ><br>2. Time to intubation <br/ ><br>3. number of attempts <br/ ><br>4. External Laryngeal manipulation required <br/ ><br>5. Cormack & Lehane grade <br/ ><br>6. POGO score <br/ ><br>7. Degree of difficulty of intubation on Likert scale <br/ ><br>8. Adverse effect / complication if anyTimepoint: At baseline <br/ ><br>