Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Group T (Topical Lignocaine): 2 sprays of 10% lignocaine (10 mg/spray) applied to either side of the oropharynx (total 40 mg), administered 3 minutes prior to IV Propofol injection, fol
Sponsors
Mahatma Gandhi Medical College and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients who are willing to participate in this study by written and informed consent. 3.Patients of either sex having age 18-65years. 4.Patient with American Society of anaesthesiologists (ASA) Class I, II
Exclusion criteria
Exclusion criteria: 1. BMI greater than 35 2. Mallampati grade 3 or above 3. Restricted neck movement 4. Loose tooth 5. Mouth opening less than 2.5 cm 6. History of allergy to lignocaine 7. Upper respiratory tract infection 8. Patients undergoing oral surgeries 9. Pregnant and lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Ease of I-gel insertion assessed by insertion score (1=Easy, 2=Moderate, 3=Difficult), number of insertion attempts, and presence of airway reflexes (cough, gag, laryngospasm)Timepoint: At the time of I-gel insertion and up to 5 minutes post-insertion | — |
Secondary
| Measure | Time frame |
|---|---|
| Hemodynamic parameters (Heart rate, Systolic blood pressure, Diastolic blood pressure, Mean arterial pressure, SpO2)Timepoint: Baseline, post-propofol induction, 1 min, 2 min and 5 min after I-gel insertion;Postoperative sore throatTimepoint: At 4 hours and 8 hours after surgery;Incidence of laryngospasm and desaturationTimepoint: Intraoperative and immediate postoperative period | — |
Countries
India
Contacts
Public ContactDr Khayyam Moin
Mahatma Gandhi Medical College and Hospital
Outcome results
None listed