Observational study comparing the safety and efficacy of Igel Supraglottic airway device insertion in anaesthetised patients by Anesthesia faculty versus residents

Not yet recruiting

• Conditions: Medical and Surgical,

• Registration Number: CTRI/2021/12/038679
• Lead Sponsor: Department of Anesthesiology

Brief Summary

This is an observational study comparing the safety and efficacy of Igel supraglottic airway device  in anaesthetised  patients by Anesthesia faculty versus residents, to study ease of insertion and learning curve associated with Igel use.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2021-12-15
• Study Start: 2022-01-14

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• ASA grade I-II fit patients.
• Patients posted for elective surgery under GA requiring I-gel Supraglottic Airway device insertion.
• Availability of informed consent and willingness of the patient to be a part of the study.

Exclusion Criteria

• Patients belonging to ASA grade III-IV 2.
• Patients with cardiac, neurological and respiratory diseases.
• Patients with full stomach.
• Emergency case patients.
• Patients scheduled for head and neck surgery.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To observe the haemodynamic parameters at the time of Igel insertion	5 minutes

Secondary Outcome Measures

Name	Time	Method
To observe any complications during and after the insertion.
To compare the number of attempts taken for successful insertion of i-gel as well as the time taken to do so by each group.

Trial Locations

Locations (1)

Dr. D.Y Patil Medical College Hospital and Research Centre; 🇮🇳 Pune, MAHARASHTRA, India

Dr. D.Y Patil Medical College Hospital and Research Centre

🇮🇳Pune, MAHARASHTRA, India

Dr Dipanjali Mahanta

Principal investigator

9673586122

dipanjalimahanta@gmail.com