Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Aerosol generated in endotracheal tube and while inserting proseal laryngeal mask will be measured: Aerosol produced while intubating with endotracheal tube or proseal laryngeal mask an
Sponsors
Department of Anaesthesiology and Intensive Care
Eligibility
Inclusion criteria
Inclusion criteria: adults of ASA 1 and 2
Exclusion criteria
Exclusion criteria: 1.mouth opening 2.cervical spine fracture 3.gross anatomic abnormalities of head and neck or malformations of airway 4.radiation induced scarring or post burn contracture of perioral region or neck airway 5. edentulous patients 6.pregnant female 7. full stomach patient, hiatus hernia, gastroesophageal reflus 8. difficult laryngoscopy amd intubation 9. bony abnormalities of cervicalspine or TM joint
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluating and comparing quantitative assessment of aerosol generation in terms of number (ug/cumm) and concentration per litre using Proseal laryngeal mask airway and endotracheal tubeTimepoint: 1. Baseline 2. After endotracheal tube or proseal laryngeal mask insertion | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Time taken for aerosol particle after intubation using Proseal laryngeal mask airway or endotracheal tube to return to the baseline value and will be noted in minutes. 2. Time taken to decrease aerosol particle after extubation using Proseal laryngeal mask airway or endotracheal tube to return to the baseline value and will be noted in minutes.Timepoint: After extubation, serial recordings will be taken till the aerosol concentration comes to baseline and that time will be noted | — |
Countries
India
Contacts
Public ContactNeelam Prasad
Maualana Azad Medical College
Outcome results
None listed