Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Dexmedetomidine 0.5mcg/kg: Study participants will be randomized into two groups.
Intervention group will receive 0.5mcg/kg Dexmedetomidine before induction
Control Intervention1: Fenta
Sponsors
A SUDARSHAN
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients aged between 18-60 years 2. American Society of Anaesthesiologists Physical Status 1 & 2 3. Patients undergoing general anaesthesia for elective surgical procedures
Exclusion criteria
Exclusion criteria: 1.Patients not willing to participate in the study 2. Patients with reduced mouth opening 3. Neck and Facial burns and contracures 4. Modified Mallampati class more than 3 5. Body Mass Index more than 30 6. Thyromental distance less than 6cms 7. Upper and Lower airway obstruction 8. Patients on beta blockers 9. Patients with known allergy to study drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Objective of this study to assess the effects of dexmedetomidine and fentanyl on the ease of insertion and hemodynamic changes on placement of i-gelTimepoint: Objective of this study to assess the effects of dexmedetomidine and fentanyl on the ease of insertion on placement of i-gel and hemodynamic changes on placement of i-gel after 1minute and 3minutes and 5minutes and 10minutes after the placement of i-gel | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: | — |
Countries
India
Contacts
Public ContactDr N RATAN SINGH
REGIONAL INSTITUTE OF MEDICAL SCIENCES
Outcome results
None listed