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Comparison between two devices for securing airway access in patients undergoing general anaesthesia

Not Applicable
Completed
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/02/049457
Lead Sponsor
Pt.B.D.Sharma University of Health Sciences PGIMS, Rohtak, Haryana
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
90
Inclusion Criteria

90 patients belonging to American Society of Anaesthesiologists(ASA) I or II scheduled for elective surgery under general anaesthesia requiring endotracheal intubation.

Exclusion Criteria

Patients having respiratory or pharyngeal pathology, mouth opening <2.5cms, body mass index >30kg/m2, pregnancy, full stomach, anticipated difficult airway and any patient who refuses to participate in the study will be excluded from the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Success of Intubation through the LMA and comparison between 2 devices - LMA Blockbuster and ProtectorTimepoint: Baseline(T0)-MAP(mmHg),HR(min),spO2(%) <br/ ><br>After Induction(T1)- <br/ ><br>MAP(mmHg),HR(min),spO2(%) <br/ ><br>After Insertion(T2)- <br/ ><br>MAP(mmHg),HR(min),spO2(%) <br/ ><br>After Intubation(T3)- <br/ ><br>MAP(mmHg),HR(min),spO2(%)
Secondary Outcome Measures
NameTimeMethod
Success of placement of LMA <br/ ><br>Time taken for LMA insertion <br/ ><br>Oropharyngeal Seal pressures <br/ ><br>Number of attempts and ease of intubation <br/ ><br>Hemodynamic variations <br/ ><br>Any special manouvres used <br/ ><br>Post-operative complicationsTimepoint: Assessment of Mean Arterial Pressures, Heart Rate and Oxygen saturation will be done at Baseline, at Induction, at Insertion of supraglottic device and after Intubation. Post-operative complications-immediately,after half hour and after 1 hour will be assessed. Data compiled and appropriate statistical tests will be applied to analyse the results.
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