Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Lignocaine for treatment of propofol infusion pain: Inj lignocaine will be given at a dose of 0.5mg/kg IV STAT after propofol insuion
Control Intervention1: combination of lignocaine an
Sponsors
Armed Forces Medical College Pune
Eligibility
Inclusion criteria
Inclusion criteria: ASA status I and II Patients requiring intravenous sedation with propofol
Exclusion criteria
Exclusion criteria: patients with allergies to propofol patients on long term corticosteroid therapy patients with history of significant cardiovascular, hepatic or renal disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| incidence of pain experienced during propofol injection using 4 pointer verbal rating scale among groups pretreated with lignocaine, combination of lignocaine and dexamethasone with standard treatment of care which is saline and propofolTimepoint: incidence of pain experienced during propofol injection using 4 pointer verbal rating scale among groups pretreated with lignocaine, combination of lignocaine and dexamethasone after 10 second of propofol injection | — |
Secondary
| Measure | Time frame |
|---|---|
| the intensity of pain using 4 pointer verbal rating scale, hemodynamic parameters and behavioural signs of discomfort among groups pretreated with lignocaine, combination of lignocaine and dexamethasone with standard treatment of care which is saline and propofolTimepoint: 18 months | — |
Countries
India
Contacts
Public ContactDr Dewendra Gajbhiye
Guide
Outcome results
None listed