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Assessment of endotracheal tube placement using Ambu Aura 40 versus Ambu Aura i" supraglottic devices as conduit

Not yet recruiting
Conditions
Medical and Surgical,
Registration Number
CTRI/2023/06/053354
Lead Sponsor
Pt BD Sharma PGIMS Rohtak
Brief Summary

This prospective ,randomised , single  blinded study will be conducted in the Department of Anaesthesiology and Critical Care,Pt.B.D.Sharma PGIMS,Rohtak . Sixty patients of either sex aged 18 to 60 years belonging to ASA Grade 1 and 2 undergoing surgical procedures requiring intubation will be included in this study.All the patients will be examined pre operatively and details of the clinical history ,general physical examination and systemic examination will be recorded . Detailed examination of the patients will be carried out for any neck mass ,any loose tooth,mouth opening .Routine investigations like hemoglobin,bleeding time,clotting time and complete urine examination will be carried out in all the patients .Any other relevant investigation like blood urea ,srum creatinine ,serum electrolytes, chest x-ray and ECG will be done as and when required.Patient will be explained about the procedure and written and informed consent will be obtained for participation in the study.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Sixty adult patients aged between 18-60 years of either sex of ASA grade I and II scheduled for elective surgery requiring general anaesthesia will be included.

Exclusion Criteria

patients refusing to participate,having respiratory or pharyngeal pathology,mouth opening <2.5 cms ,body mass index>30kgm² ,pregnancy,full stomach,suspected difficult airway will be excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the ease and success of endotracheal tube placement through ambu aura 40 versus.ambu aura i. maximum of 3 attempts. expected to be within 30 secondstime for insertion of device(within 10 sec), Time for insertion of tube (within 20 sec), Hemodynamic parameters at Baseline, At time of induction, at supraglottic insertion, At Tube insertion, after 5 min
Secondary Outcome Measures
NameTimeMethod
Time taken for placement of SAD and intubation through SADPosition of SAD confirmed with Fiberoptic

Trial Locations

Locations (1)

Pt ,B.D.Sharma PGIMS ,Rohtak

🇮🇳

Rohtak, HARYANA, India

Pt ,B.D.Sharma PGIMS ,Rohtak
🇮🇳Rohtak, HARYANA, India
Dr Nisha
Principal investigator
7082700162
93yadavnisha@gmail.com

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