None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients aged 18-60 years of either sex. 2. American Society of Anaesthesiologist Physical Status I and II. 3. Patients willing to be a part of the study.
Exclusion criteria
Exclusion criteria: 1. Patients refusal or unwillingness to be a part of the study 2. American Society of Anaesthesiologist Physical Status III and IV. 3. Allergy to Ketamine. 4. History of major psychiatric disorder or History of substance abuse. 5. Systemic illnesses involving cardiovascular, nervous or respiratory system, any renal or liver diseases. 6. Hemodynamically unstable patient. 7. Pregnancy 8. Anticipated difficult airway or more than one attempt for intubation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the efficacy of intracuff versus nebulized ketamine in preventing post-operative sore throatTimepoint: 0 MIN 1 HOUR 2 HOUR 4 HOUR 8 HOUR 12 HOHR 18 HOUR 24 HOUR | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the incidence and severity of postoperative sore throat in patients administered intracuff ketamine.Timepoint: 0 MIN 1 HOUR 2 HOUR 4 HOUR 8 HOUR 12 HOHR 18 HOUR 24 HOUR;To assess the incidence and severity of postoperative sore throat in patients administered ketamine nebulization.Timepoint: 0 MIN 1 HOUR 2 HOUR 4 HOUR 8 HOUR 12 HOHR 18 HOUR 24 HOUR;To compare the incidence and severity of postoperative hoarseness of voice and postoperative cough between both the groups.Timepoint: 0 MIN 1 HOUR 2 HOUR 4 HOUR 8 HOUR 12 HOHR 18 HOUR 24 HOUR;To observe the adverse effects associated with the study drug, if any.Timepoint: 0 MIN 1 HOUR 2 HOUR 4 HOUR 8 HOUR 12 HOHR 18 HOUR 24 HOUR | — |
Countries
India
Contacts
Shri Ram Murti Smarak Institute of Medical Sciences