None listed
Conditions
Interventions
Intervention1: concentrations of propofol 1% affect the intensity of pain
at the injection site during anaesthesia in adult patients undergoing surgery?: The 1% propofol 02ml will be injected through
Sponsors
Anuranjana Lucka
Eligibility
Inclusion criteria
Inclusion criteria: ASA I & II patients 20 years to 60 years
Exclusion criteria
Exclusion criteria: Patients who deny consent Patients with a known history of allergy or hypersensitivity to propofol or any of its components ASA 3 and 4 Patients with cardiac respiratory renal or hepatic disease Patients with peripheral intravenous cannula of size 22G or narrower
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the pain experienced at the injection site in patients undergoing general anaesthesia with propofol at dilutions of 1%, 0.5% and 0.33%Timepoint: To compare the pain experienced at the injection site in patients undergoing general anaesthesia with propofol at dilutions of 1%, 0.5% and 0.33% at 00min and 01min after injection | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the association between propofol dilutions and the occurrence of local side effects such as vascular irritation swelling To assess any differences in hemodynamic parameters heart rate and blood pressure among the different dilutionsTimepoint: access at 0min 1min 5min | — |
Countries
India
Contacts
Public ContactSurabhi S Raghav
Armed forces medical college
Outcome results
None listed