COMPARATIVE STUDY BETWEEN I-GEL AND LMA-CLASSIC IN ANAESTHETISED, SPONTANEOUSLY BREATHING ADULT PATIENTS UNDERGOING ELECTIVE SURGICAL PROCEDURES

Not Applicable

• Conditions: Health Condition 1: null- American Society of Anaesthesiologists (ASA) grade I-II

• Registration Number: CTRI/2018/06/014506
• Lead Sponsor: KPC MEDICAL COLLEGE AND HOSPITA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

INCLUSION CRITERIA

The surgical procedures taken into consideration are

1)Adult patients of either sex aged between (15-60) years.

2)American Society of Anaesthesiologists (ASA) grade I-II

3)Mallampatti (MP) grade I and II

4)Body Mass Index (BMI) between (20-25) kg/m²

5)Scheduled for elective surgeries under general anaesthesia, not requiring muscle relaxation.

Exclusion Criteria

EXCLUSION CRITERIA

The following patients will be excluded from the study

1)Age < 15 years and > 60 years.

2)American Society of Anaesthesiologists (ASA) grade III and IV

3)Mallampatti (MP) grade 3 and 4

4)Patients having any abnormality of the neck, anticipated difficult airway.

5)Mouth opening < 2 cm.

6)Upper respiratory tract infection.

7)History of Obstructive Sleep Apnoea.

8)Obese patients with Body Mass Index (BMI) > 28 kg/m²

9) Patients with increased risk of aspiration.

10) Duration of surgery > 1 hour.

11) Pregnant females.

12) Patients with reported history of hypersensitivity for one or more medications and latex.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
PRIMARY OBJECTIVES <br/ ><br>To study and compare two supraglottic airway devices, I-gel and Classical laryngeal mask airway, in anaesthetized adult patients with spontaneous ventilation during elective surgical procedures, with respect to <br/ ><br>1)Time taken for insertion. <br/ ><br>2)Number of insertion attempts. <br/ ><br>3)Ease of insertion, any manipulations required. <br/ ><br>Timepoint: 2 years

Secondary Outcome Measures

Name	Time	Method
ILTimepoint: NI