trial of breathing tube through two airway devices
Phase 3
Completed
- Conditions
- Health Condition 1: null- patients of either sex, in the age group 18 â?? 60 years belonging to ASA physical status I-II, weighing 50 â?? 90 kg and scheduled for elective surgical procedures requiring tracheal intubation
- Registration Number
- CTRI/2016/06/006997
- Lead Sponsor
- Post Graduate Institute of Medical Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
ASA physical status I-II,weighing 50 â?? 90 kg and scheduled for elective surgical procedures requiring tracheal intubation were included in the study.
Exclusion Criteria
ASA III-V patients,
contraindication to use of muscle relaxants, anticipated or known difficult intubation or ventilation and
patients at increased risk of aspiration or having a history of symptomatic gastroesophageal reflux or hiatal hernia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of successful intubation in first attemptTimepoint: number of successful intubation in first attempt. After intubation through the airway device whether ETCO2 graph appears or not was noted in first attempt( If ETCO2 graph detected on the monitor, intubation was considered successful)
- Secondary Outcome Measures
Name Time Method overall success rate, ease of SGA insertion and intubation, time to SGA insertion and intubation and adverse events.Timepoint: Time taken to insert the airway was noted from holding the device to successfully inserting the device. Time taken to intubation was noted from holding the tube in hand to successful intubation. i e appearance of ETCO2 curve on the monitor. Adverse events like sore throat, horseness, vocal cord paralysis was assessed soon after extubation and 24 hours after the procedure