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Comparison of blind approach with direct vision for successful intubation through airway device in adult patients undergoing surgery.

Phase 3
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/04/065357
Lead Sponsor
Department of Anaesthesiology Intensive Care
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All patients belonging to American Society of Anaesthesiologists (ASA) grade I & II; aged between 18yrs to 60yrs of both the genders, undergoing elective surgery of less than 3 hours anticipated duration of surgery requiring General Anaesthesia with orotracheal intubation with supine position intra-operatively.

Exclusion Criteria

•Predicted difficult airway

•Increased aspiration risk- Recent trauma, full stomach, pregnancy, intestinal obstruction, gastroesophageal reflux disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the first pass success rate of blind intubation with that of fiberoptic guided intubation through BlockbusterTM laryngeal mask airway device, using polyvinyl chloride endotracheal tube.Timepoint: Preop, at time of insertion of blockbuster LMA, at time of endotracheal intubation thorugh blockbuster LMA, 1 min after insertion, 3 min after insertion, 5 min after insertion, 10 min after insertion, at time of extubation & in post anaesthesia care unit
Secondary Outcome Measures
NameTimeMethod
I.Endotracheal tube Insertion characteristics <br/ ><br> <br/ ><br> a)Ease of insertion <br/ ><br> b)Number of attempts for successful intubation <br/ ><br> c)Time taken for intubation <br/ ><br> d)Manuevers required for tube insertion <br/ ><br> <br/ ><br>II.Hemodynamic changes – Blood Pressure(Systolic Blood <br/ ><br> Pressure/Diastolic Blood Pressre), Heart Rate, Oxygen <br/ ><br> Saturation changes <br/ ><br>Timepoint: Hemodynamics changes as secondary outcome will be measured : Preop, at time of insertion of blockbuster LMA, at time of endotracheal intubation thorugh blockbuster LMA, 1 min after insertion, 3 min after insertion, 5 min after insertion, 10 min after insertion, at time of extubation & in post anaesthesia care unit
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