Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Control Intervention1: Low dose Ketamine and Lignocaine: Dose :Group K patients receive 100mcg/kg of ketamine intravenously and Group L patients receive 0.5 mg/kg of 2% lignocaine intravenously withou
Sponsors
Dr Aravind
Eligibility
Inclusion criteria
Inclusion criteria: 1.ASA 1 and 2 patients 2.Age more than 18 years 3.Patients undergoing general anaesthesia 4.Patients acceptance 5.Patients with Propofol as induction agent
Exclusion criteria
Exclusion criteria: 1.Patients allergic to Propofol and Ketamine 2.Patients allergic to egg 3.Patietns with cardiovascular, neurologica and respiratory diseases 4.ASA 3 and 4 5.Emergency Surgeries
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this study is to compare the effect of low dose ketamine and 2% lignocaine pretreatment in preventing pain on propofol injection (POPI ) with verbal rating scale ( 0-3 ) and its haemodynamic responses. Timepoint: The primary outcome of this study is to compare the effect of low dose ketamine and 2% lignocaine pretreatment in preventing pain on propofol injection (POPI ) with verbal rating scale ( 0-3 ) and its haemodynamic responses. Assessed during injection, o minute, 1,2,3 and 5 minutes and the outcome is predicted. | — |
Secondary
| Measure | Time frame |
|---|---|
| Haemodynamic parameters like heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure and oxygen saturation monitoredTimepoint: every one minute till 10 minutes | — |
Countries
India
Contacts
Public ContactR Arun Kumar
PSG IMSR, Coimbatore, India
Outcome results
None listed