Health Condition 1: O- Medical and Surgical Health Condition 2: null- Propofol injection pain
Conditions
Interventions
Intervention1: Intravenous injection of lignocaine, lignocaine and dexamethasone combination before propofol induction: pain after propofol injection will be evaluated.
Control Intervention1: lignocai
Sponsors
Dr Chetna Umrigar
DrSmita R Engineer
Eligibility
Inclusion criteria
Inclusion criteria: ASA status I, II Patients who required general anaesthesia
Exclusion criteria
Exclusion criteria: 1.ASA status III, IV, V 2.Hypersensitivity reaction to study drug, soyabean oil, glycerol, egg lecithin 3.Pregnant or lactating patients 4.Patients with history of chronic pain with neurologic, psychiatric, cardiac, renal or liver disease or taking sedative or analgesic preoperatively
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| (1) Withdrawal response score(2) Verbal rating score (3) Behavioral signsTimepoint: Pain intensity will be evaluated during 10 second pause up to 120seconds before induction of anaesthesia | — |
Secondary
| Measure | Time frame |
|---|---|
| pulse, NIBP, SP02, ECGTimepoint: Hemodynamic data will be recorded as basal ,after premedication ,pulse and spo2 at every 10 seconds interval for 60 seconds after injecting study drug ,after releasing cuff ,induction and every 5 minutes for 20 min.;Subjects will be contacted for 24â??h following surgery and questioned about pain, edema, wheal, flare response or swelling at the injection site.Timepoint: 24 hours after surgery | — |
Countries
India
Contacts
Public ContactDr Chetna Umrigar
B.J.Medical college
Outcome results
None listed