None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Doctors and Paramedical staff from a multidisciplinary team working in a tertiary care super speciality Paediatric centre converted into a COVID care centre. 2.No experience on any of the video laryngoscope
Exclusion criteria
Exclusion criteria: 1.Previous experience of intubating in a similar setting (i.e. with video laryngoscope within an intubation box 2.Refuse to give consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The Primary endpoint of this study is to compare the time to intubation between the two groups. Group 1 McGrath and Group 2; C-MACTimepoint: One month | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare parameters- Cormack-Lehane grading, Percentage of Glottic opening, Failed intubation, First attempt success rate and Ease of intubation by the user.Timepoint: one month | — |
Countries
India
Contacts
Post Graduate Institute of Child health Noida