Health Condition 1: 3- Administration
Conditions
Interventions
Intervention1: Ketamine: inj.ketamine 0.5mg/kg (Group K) diluted with normal saline loaded in 10ml syringe administered over 10mins prior to Propofol injection pain.
Control Intervention1: Dexmedetomi
Sponsors
M S Ramaiah Medical College
Eligibility
Inclusion criteria
Inclusion criteria: ASA 1/2 undergoing elective surgery under general anaesthesia
Exclusion criteria
Exclusion criteria: CV disease and uncontrolled HTN, allergy to study drugs, hepatic/renal issues, pregnancy, psychiatric illness or problem in communication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the degree of propofol injection pain between the two groups receiving ketamine v/s dexmedetomidine. Timepoint: over a 20sec duration during injection of Propofol | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the hemodynamic changes like heart rate ,blood pressure, oxygen saturation following the pretreatment with ketamine v/s dexmedetomidine. Timepoint: At baseline, during infusion of Dexmedetomidine or Ketamine over 10mins, prior to adminstration of propofol. | — |
Countries
India
Contacts
Public ContactDr Leena H Parate
M S Ramaiah Medical College
Outcome results
None listed