None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.ASA grade I or II fit patients. 2. Patients aged between 18 and 60 years of age. 3. Patients undergoing surgeries under general anaesthesia. 4. Haemodynamically stable patients with all routine investigations within normal limits and without any comorbidities. 5.Written informed consent from the concerned patient.
Exclusion criteria
Exclusion criteria: 1.Patients who are not willing to participate in the study. 2.Patients with ASA grade III and above physical status. 3.Patients who are aged less than 18 and more than 60 years of age. 4. Patients who are posted for emergency procedures. 5. Patients with known allergy to the study drugs. 6. Patients with difficult intubation. 7. Patients who are obese. 8. Patients who have psychiatric, neurological, neuromuscular or cardiovascular disease or impairment of hepatic or renal function.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To observe the attenuation of pressor responses to laryngoscopy and endotracheal intubation with preoperative nebulization with dexmedetomidine and incidence of post operative sore throatTimepoint: Pre intubation, scopy 0 minutes, every 1 minute upto 10 minutes post intubation, after extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| To observe the attenuation of pressor responses to laryngoscopy and endotracheal intubation with preoperative nebulization with dexmedetomidine and incidence of post operative sore throatTimepoint: Pre intubation, scopy 0 minutes, every 1 minute upto 10 minutes post intubation, after extubation | — |
Countries
India
Contacts
Dr. D Y Patil Medical College and Research Centre, Department of Anaesthesiology