Comparative efficacy and safety of two supraglottic airway devices during general anaesthesia in childre
Not Applicable
- Conditions
- Health Condition 1: null- ASA I and II children below 1 year of age posted for ophthalmic surgery of 20 min-2 hr duration
- Registration Number
- CTRI/2018/06/014473
- Lead Sponsor
- Department of Anaesthesiology Pain medicine and Critical care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Infants below 1yr. of age
Posted for Only elective ophthalmic surgery
ASA I & II patients
Duration of surgery (20 mins-2 hrs)
Exclusion Criteria
All patients above 1 year of age
Not willing to consent (Consent taken from parents)
Infants with any-airway anomalies, active URTI, known difficult airway, lung disease requiring high PEEP
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oropharyngeal Leak Pressure (in cm H2O)Timepoint: Oropharyngeal leak pressure will be measured at 3 times: after insertion and fixation of the device, 10 min after insertion and at the end of surgery
- Secondary Outcome Measures
Name Time Method 1. First insertion success rate <br/ ><br>2. Time to insert (in seconds) <br/ ><br>3. No. of attempts for successful insertion <br/ ><br>4. Fibreoptic bronchoscopic view of glottis through the supraglottic airway device <br/ ><br>5. Post op. Complications (repeated episodes of cough, laryngospasm, desaturation) <br/ ><br> <br/ ><br>Timepoint: Time to Insert- Time between picking up the device and chest rise with PPV <br/ ><br>Fibre-optic bronchoscopic (FOB) view-breathing system will be briefly disconnected after insertion and confirmation of device <br/ ><br>and a 3-mm fiberscope will be inserted through the airway port to evaluate glottic view. <br/ ><br>Post-operative Complications- Blood stain on device (oropharyngeal trauma), repeated episodes of cough, laryngospasm, bronchospasm or desaturation will be noted after removal of device at the end of surgery <br/ ><br>