None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Informed consent patients 2. ASA Physical status grade I and II 3. Patients aged between 18 to 60 years of either gender 4. Patients undergoing elective short surgical procedures of duration 1 to 2 hours under GA with I-gel insertion
Exclusion criteria
Exclusion criteria: 1. Obese (Body Mass Index more than 30 kg per m2) 2. Pregnant patients 3. Predicted difficult airway (Mallampati grade 3 or 4) 4. Known Hypersensitivity to study drugs 5. Significant cardiovascular, pulmonary and liver disease 6. Patients with risk of aspiration such as gastroesophageal reflux or hiatal hernia 7. Patients on anti-hypertensive and sedatives
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the quality (ease, number of attempts, time taken) of I-gel insertion between either groupsTimepoint: Baseline outcomes compared between both groups during I-gel insertion | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the haemodynamic parameters (HR, SBP, DBP) before & after I-gel insertion between either groupsTimepoint: Baseline, immediately & after 3 minutes, 5 minutes, 7 minutes & 10 minutes of I-gel insertion;To compare the incidence of post-operative sore throat after I-gel insertion between either groups Timepoint: Immediately & after 24 hours of I-gel insertion | — |
Countries
India
Contacts
Heritage Institute of Medical Sciences