A study to compare two airway devices in patients with fixed neck.

Phase 4

Completed

Conditions: Calculus of gallbladder with acutecholecystitis, (2) ICD-10 Condition: K403||Unilateral inguinal hernia, with obstruction, without gangrene, (3) ICD-10 Condition: K36||Other appendicitis, (4) ICD-10 Condition: K605||Anorectal fistula,

Registration Number: CTRI/2019/06/019782

Lead Sponsor: Department of Anaesthesiology and Critical Care

Brief Summary: The aim and objectives of the thesis is to evaluate and compare endotracheal intubation through two supraglottic airway devices, Air Q Intubating Laryngeal Airway and Intubating Laryngeal Mask Airway as intubation conduit in patients with simulated fixed cervical spine. Adult patient, 18 to 60 years of age of either sex, ASA physical status I and II, scheduled for elective surgery under general anaesthesia requiring intubation. Total of 88 patients, 44 in each group will be studied. The success rate of intubation in both the groups, time taken for intubation, number of attempts, fiberoptic grading, haemodynamic changes and complications if any will be assessed. Data will be compiled and appropriate statistical test will be done to analyse the result.

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: All

Target Recruitment: 88

Inclusion Criteria

Adult patient 18 to 60 years of age of either sex , ASA physical status I or II , scheduled for elective surgery under general anaesthesia requiring intubation .

Exclusion Criteria

Patients at risk of gastric content aspiration , anticipated difficult airway, interincisor gap <2.5cm , BMI >30, poor lung compliance and abnormal oropharyngeal anatomy .

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Success rate of intubation.	The following will be assessed for both Air Q and Intubating Laryngeal Mask Airway . Data will be compiled and appropriate statistical test will be used to analyse the results
3. Time taken for insertion of device and intubation.	The following will be assessed for both Air Q and Intubating Laryngeal Mask Airway . Data will be compiled and appropriate statistical test will be used to analyse the results
2. Number of attempts.	The following will be assessed for both Air Q and Intubating Laryngeal Mask Airway . Data will be compiled and appropriate statistical test will be used to analyse the results
5. Fibre optic grading .	The following will be assessed for both Air Q and Intubating Laryngeal Mask Airway . Data will be compiled and appropriate statistical test will be used to analyse the results
7. Adverse effects .	The following will be assessed for both Air Q and Intubating Laryngeal Mask Airway . Data will be compiled and appropriate statistical test will be used to analyse the results
4. Ventilation through device.	The following will be assessed for both Air Q and Intubating Laryngeal Mask Airway . Data will be compiled and appropriate statistical test will be used to analyse the results
6. Haemodynamic parameters.	The following will be assessed for both Air Q and Intubating Laryngeal Mask Airway . Data will be compiled and appropriate statistical test will be used to analyse the results

Secondary Outcome Measures

Name	Time	Method
1. Success rate of intubation.	2. Number of attempts.

Trial Locations

Locations (1): Pt. B. D. Sharma, PGIMS , ROHTAK
🇮🇳
Rohtak, HARYANA, India
Pt. B. D. Sharma, PGIMS , ROHTAK
🇮🇳Rohtak, HARYANA, India
Dr Jasmine
Principal investigator
7896567209
j.basumatary50@gmail.com