Observational study comparing the safety and efficacy of Igel Supraglottic airway device insertion in anaesthetised patients by Anesthesia faculty versus residents
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/12/038679
- Lead Sponsor
- Department of Anesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA grade I-II fit patients.
2. Patients posted for elective surgery under GA requiring I-gel Supraglottic Airway device insertion.
3. Availability of informed consent and willingness of the patient to be a part of the study.
Exclusion Criteria
1. Patients belonging to ASA grade III-IV
2. Patients with cardiac, neurological and respiratory diseases.
3. Patients with full stomach.
4. Emergency case patients.
5. 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 insertionTimepoint: 5 minutes
- Secondary Outcome Measures
Name Time Method 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. <br/ ><br> <br/ ><br>Timepoint: 5 minutes;To observe any complications during and after the insertion. <br/ ><br>Timepoint: 20 minutes