Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: lignocaine 4% nebulization: Group L will receive lignocaine 4% nebulization( 2ml lignocaine 4% + 3ml saline) 15 min prior to induction in pre
op room.
Intervention2: ketamine 50 mg: Gr
Sponsors
Department of Anaesthesiology
Eligibility
Inclusion criteria
Inclusion criteria: Patients with American Society of Anesthesiologists (ASA) class I or class II physical status.
Exclusion criteria
Exclusion criteria: 1. Patient refusal , 2. Pateints with ASA physical status III & IV, 3. History of allergic reactions to local anaesthetics or ketamine, 4. Patient with anticipated difficult intubation, 5. Duration of intubation more than 30s or more than 1 attempt of intubation, 6. Patients undergoing oral, head and neck surgeries, 7. Duration of surgery > 2hr
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence and severity of sore throat in first 24 hours of post operative periodTimepoint: Sore throat monitoring and grading will be done at 0,1, 2, 4, 8, 12, 16 and 24 hours post-extubation by an anaesthetist not aware of the group of patients | — |
Secondary
| Measure | Time frame |
|---|---|
| To report any complication or side effect due to nebulization of lignocaine and ketamine if seenTimepoint: Monitoring will be done at 0, 2, 4, 8, 12, and 24 hours post-extubation by an anaesthetist. | — |
Countries
India
Contacts
Public ContactSwapnil Kumar Barasker
Sri Aurobindo Medical College and PG Institute
Outcome results
None listed