Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: LIGNOCAINE: INJ.LIGNOCAINE 2% 0.5mg/kg
Control Intervention1: PROPOFOL
: INJ.PROPOFOL 2-2.5mg/kg
Sponsors
Jss Academy of Higher Education and Research
Eligibility
Inclusion criteria
Inclusion criteria: 1.ASA physical status I and II patients of either sex between the age of 18-60 years 2.Patients undergoing elective surgery under general anaesthesia
Exclusion criteria
Exclusion criteria: 1.Patient with a history of allergy to egg 2.Pregnant and lactating women 3.Patients with any open wounds/fractures at the site of injection site. 4.Patients receiving pre-emptive analgesia/ analgesic intake 12 hrs prior to the surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary objective of the study is to compare which of the two methods is superior / more effective in reducing or preventing pain associated with the injection of propofol in patients who are undergoing general anaesthesia.Timepoint: From beginning of general anaesthesia till post operative recovery period | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary objective includes assessment of the vital signs (blood pressure, heart rate, respiratory rate & o2 saturation) in all participant To assess the severity of pain at the injection site among healthy adults undergoing general anaesthesia Timepoint: From beginning of general anaesthesia till post operative recovery period | — |
Countries
India
Contacts
Public ContactDr Vyshnavi S
Jss Academy of Higher Education and Research
Outcome results
None listed