None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.The patient who are undergoing general anaesthesia and eligible cases during the study period are covered 2.American Society of Anaesthesiologist physical status (ASA PS) I and II 3.BMI 18-24 Kg/m2
Exclusion criteria
Exclusion criteria: 1.Allergy to study medication 2.Serious venous insufficiency 3.Pregnant/lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence and severity of pain on propofol injection in patients pretreated with cold saline, lignocaine, cold saline + lignocaine and normal saline using pain scoreTimepoint: pain score is taken Immediately after giving 5ml of propofol injection (within 5 to 10 seconds) | — |
Secondary
| Measure | Time frame |
|---|---|
| Post operative recall of pain on propofol injection in patients pretreated with cold saline, lignocaine, cold saline + lignocaine and normal salineTimepoint: post-operatively patient will grade pain using numerical rating scale when fully conscious within 1-2 hours | — |
Countries
India
Contacts
Yenepoya Medical College and Hospital